Panic Disorder Without Agoraphobia

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Results for "Panic Disorder Without Agoraphobia": 45 genes, 1001 gene sets

Name
PAND1 Gene Panic disorder 1
PAND2 Gene panic disorder 2
PAND3 Gene panic disorder 3
OS4 Gene Osteoarthritis, generalized, without* dysplasia, susceptibility to*
TNFRSF10C Gene tumor necrosis factor receptor superfamily, member 10c, decoy without* an intracellular domain* The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains an extracellular TRAIL-binding domain and a transmembrane domain, but no cytoplasmic death domain. This receptor is not capable of inducing apoptosis, and is thought to function as an antagonistic receptor that protects cells from TRAIL-induced apoptosis. This gene was found to be a p53-regulated DNA damage-inducible gene. The expression of this gene was detected in many normal tissues but not in most cancer cell lines, which may explain the specific sensitivity of cancer cells to the apoptosis-inducing activity of TRAIL. [provided by RefSeq, Jul 2008]
CTEPH1 Gene Pulmonary hypertension, chronic thromboembolic, without* deep vein thrombosis, susceptibility to*
MGR3 Gene Migraine, familial, with or without* aura, susceptibility to*
MGR5 Gene Migraine with or without* aura, susceptibility to, 5*
LILRA3 Gene leukocyte immunoglobulin-like receptor, subfamily A (without* TM domain), member 3* This gene encodes a member of a family of immunoreceptors that are expressed predominantly in monocytes and B cells, and at lower levels in dendritic cells and natural killer cells. The encoded protein lacks the transmembrane region found in other members of this family. It acts as a soluble receptor for class I major histocompatibility complex (MHC) antigens. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and is polymorphic in human populations, with many individuals containing a deletion of this genomic region. [provided by RefSeq, Mar 2014]
RIT2 Gene Ras-like without* CAAX 2* RIN belongs to the RAS (HRAS; MIM 190020) superfamily of small GTPases (Shao et al., 1999 [PubMed 10545207]).[supplied by OMIM, Mar 2008]
RIT1 Gene Ras-like without* CAAX 1* This gene encodes a member of a subfamily of Ras-related GTPases. The encoded protein is involved in regulating p38 MAPK-dependent signaling cascades related to cellular stress. This protein also cooperates with nerve growth factor to promote neuronal development and regeneration. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]
HTGH Gene Hypertrichosis terminalis, generalized, with or without* gingival hyperplasia*
RPH3AL Gene rabphilin 3A-like (without* C2 domains)* The protein encoded by this gene plays a direct regulatory role in calcium-ion-dependent exocytosis in both endocrine and exocrine cells and plays a key role in insulin secretion by pancreatic cells. This gene is likely a tumor suppressor. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jun 2010]
ANOP1 Gene anophthalmos 1 (with mental retardation, without* limb anomalies or dental or urogenital abnormalities)*
MGR12 Gene Migraine, with or without* aura, susceptibility to, 12*
SSD Gene Speech-sound disorder
OHDS Gene Orthostatic hypotensive disorder* of Streeten*
MAFD9 Gene Major affective disorder-9, susceptibility to
MAFD8 Gene Major affective disorder-8, susceptibility to
MAFD5 Gene Major affective disorder* 5*
MAFD1 Gene major affective disorder* 1*
MAFD3 Gene Major affective disorder* 3, early onset*
MDD2 Gene Major depressive disorder* 2*
MDD1 Gene Major depressive disorder
MAFD2 Gene major affective disorder* 2*
MAFD4 Gene Major affective disorder* 4*
MAFD6 Gene Major affective disorder* 6*
ADHD2 Gene Attention deficit-hyperactivity disorder, susceptibility to, 2
HDL3 Gene Huntington-like neurodegenerative disorder* 2*
BDET Gene Bleeding disorder, east Texas type
ADHD4 Gene Attention deficit-hyperactivity disorder, susceptibility to, 4
ADHD5 Gene Attention deficit-hyperactivity disorder, susceptibility to, 5
ADHD6 Gene Attention deficit-hyperactivity disorder, susceptibility to, 6
ADHD1 Gene Attention deficit-hyperactivity disorder, susceptibility to, 1
ADHD3 Gene Attention deficit-hyperactivity disorder, susceptibility to, 2
SCZD8 Gene schizophrenia disorder* 8*
SCZD7 Gene schizophrenia disorder* 7*
SCZD6 Gene schizophrenia disorder* 6*
SCZD1 Gene schizophrenia disorder* 1*
SCZD3 Gene schizophrenia disorder* 3*
SCZD10 Gene schizophrenia disorder* 10 (periodic catatonia)*
NDNC9 Gene Nail disorder, nonsyndromic congenital, 9
CLA3 Gene cerebellar ataxia 3 (cerebellar parenchyma disorder* 1)*
SCZD2 Gene schizophrenia disorder* 2*
PDR Gene pigment disorder, reticulate
Panic Disorder Without Agoraphobia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Panic Disorder Without Agoraphobia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Panic Disorder With Agoraphobia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Panic Disorder With Agoraphobia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
anxiety disorder; depressive disorder, major; panic disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety disorder; depressive disorder, major; panic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
major depressive disorder and panic disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease major depressive disorder and panic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anorexia nervosa, attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, or Tourette syndrome (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anorexia nervosa, attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, or Tourette syndrome (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Panic Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Panic Disorder from the curated CTD Gene-Disease Associations dataset.
Panic Disorder Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Panic Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
panic disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease panic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
panic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease panic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
schizophrenia; panic disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; panic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
panic disorder; migraine Gene Set From GAD Gene-Disease Associations genes associated with the disease panic disorder; migraine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
panic disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease panic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
panic disorder and anxious personality Gene Set From GAD Gene-Disease Associations genes associated with the disease panic disorder and anxious personality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Panic disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Panic disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
panic disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease panic disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Panic Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Panic Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
panic disorder 3 Gene Set From OMIM Gene-Disease Associations genes associated with the panic disorder 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
panic disorder 2 Gene Set From OMIM Gene-Disease Associations genes associated with the panic disorder 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
panic disorder syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the panic disorder syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{panic disorder, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {panic disorder, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Panic Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Panic Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Panic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Panic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Panic disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Panic disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Agoraphobia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Agoraphobia from the curated CTD Gene-Disease Associations dataset.
agoraphobia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease agoraphobia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
agoraphobia Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term agoraphobia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
agoraphobia Gene Set From HPO Gene-Disease Associations genes associated with the agoraphobia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Agoraphobia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Agoraphobia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Agoraphobia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Agoraphobia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Agoraphobia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Agoraphobia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Agoraphobia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Agoraphobia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
schizophrenia; depressive disorder, major; bipolar disorder; delusional disorder; psychosis Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; depressive disorder, major; bipolar disorder; delusional disorder; psychosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit disorder; conduct disorder; oppositional defiant disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit disorder; conduct disorder; oppositional defiant disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
conduct disorder; oppositional defiant disorder; antisocial personality disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease conduct disorder; oppositional defiant disorder; antisocial personality disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; attention deficit disorder; conduct disorder; oppositional defiant disorder; dementia, frontotemporal Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; attention deficit disorder; conduct disorder; oppositional defiant disorder; dementia, frontotemporal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
panic attack Gene Set From GAD Gene-Disease Associations genes associated with the disease panic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
panic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term panic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Panic Attacks Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Panic Attacks in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Panic Symptoms Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Panic Symptoms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Focal epilepsy with speech disorder with or without mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal epilepsy with speech disorder with or without mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA from the curated CTD Gene-Disease Associations dataset.
noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set From OMIM Gene-Disease Associations genes associated with the noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, focal, with speech disorder and with or without mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, focal, with speech disorder and with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
bipolar disorder; affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar disorder; affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressive disorder, major; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar disorder; unipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar disorder; unipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; alcoholism; attention deficit disorder; depression; neuroticism; affective disorder; suicidal behavior Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; alcoholism; attention deficit disorder; depression; neuroticism; affective disorder; suicidal behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizoaffective disorder; alcoholism; bipolar disorder; suicide Gene Set From GAD Gene-Disease Associations genes associated with the disease schizoaffective disorder; alcoholism; bipolar disorder; suicide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit hyperactivity disorder and conduct disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit hyperactivity disorder and conduct disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar affective disorder; unipolar affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar affective disorder; unipolar affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
conduct disorder; hyperkinetic disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease conduct disorder; hyperkinetic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antisocial personality disorder attention deficit hyperactivity disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease antisocial personality disorder attention deficit hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; bipolar disorder; affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; bipolar disorder; affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; alcohol abuse; depressive disorder, major; dermal erythema; schizoaffective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; alcohol abuse; depressive disorder, major; dermal erythema; schizoaffective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
seasonal affective disorder; premenstrual dysphoric disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease seasonal affective disorder; premenstrual dysphoric disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit disorder; seasonal affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit disorder; seasonal affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressive disorder, major; bipolar disorder; affective psychoses Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; bipolar disorder; affective psychoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; schizoaffective disorder; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; schizoaffective disorder; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressive disorder, major; bipolar disorder; suicide Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; bipolar disorder; suicide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; depressive disorder, major; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; depressive disorder, major; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety disorder; depressive disorder, major; neuroticism Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety disorder; depressive disorder, major; neuroticism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; schizoaffective disorder; affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; schizoaffective disorder; affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit disorder; conduct disorder; aggressive behavior Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit disorder; conduct disorder; aggressive behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Schizophrenia, schizoaffective disorder or bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Schizophrenia, schizoaffective disorder or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Functional impairment in major depressive disorder, bipolar disorder and schizophrenia Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Functional impairment in major depressive disorder, bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Attention deficit hyperactivity disorder and conduct disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Attention deficit hyperactivity disorder and conduct disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bipolar disorder and major depressive disorder (combined) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bipolar disorder and major depressive disorder (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bipolar disorder (age of onset <21) or attention deficit hyperactivity disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder (age of onset <21) or attention deficit hyperactivity disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bipolar disorder or attention deficit hyperactivity disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder or attention deficit hyperactivity disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Oppositional defiant disorder dimensions in attention-deficit hyperactivity disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Oppositional defiant disorder dimensions in attention-deficit hyperactivity disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Eating disorder in bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eating disorder in bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bipolar disorder and eating disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder and eating disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HIV-associated neurocognitive disorder (mild neurocognitive disorder or asymptomatic neurocognitive impairment) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HIV-associated neurocognitive disorder (mild neurocognitive disorder or asymptomatic neurocognitive impairment) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HIV-associated neurocognitive disorder (mild neurocognitive disorder) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HIV-associated neurocognitive disorder (mild neurocognitive disorder) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Functional impairment in major depressive disorder, bipolar disorder and schizophrenia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Functional impairment in major depressive disorder, bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, schizoaffective disorder or bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, schizoaffective disorder or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disruptive behavior disorder and attention deficit hyperactivity disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disruptive behavior disorder and attention deficit hyperactivity disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Attention deficit hyperactivity disorder and conduct disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Attention deficit hyperactivity disorder and conduct disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bipolar disorder or major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder or major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obsessive-compulsive disorder or autism spectrum disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obsessive-compulsive disorder or autism spectrum disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, bipolar disorder or major depressive disorder x sex interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or major depressive disorder x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, bipolar disorder or major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, bipolar disorder or major depressive disorder x sex interaction (3df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or major depressive disorder x sex interaction (3df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, bipolar disorder or recurrent major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or recurrent major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bronchiectasis with or without elevated sweat chloride 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bronchiectasis with or without elevated sweat chloride 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Woolly hair, autosomal recessive 2, with or without hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Woolly hair, autosomal recessive 2, with or without hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypogonadotropic hypogonadism 12 with or without anosmia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypogonadotropic hypogonadism 12 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy, cystic, without megalencephaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy, cystic, without megalencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cognitive impairment with or without cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cognitive impairment with or without cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypogonadotropic hypogonadism 19 with or without anosmia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypogonadotropic hypogonadism 19 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypogonadotropic hypogonadism 17 with or without anosmia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypogonadotropic hypogonadism 17 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bronchiectasis with or without elevated sweat chloride 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bronchiectasis with or without elevated sweat chloride 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, without vestibular involvement, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, without vestibular involvement, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short-rib thoracic dysplasia 11 with or without polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Testicular anomalies with or without congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Capillary malformation without arteriovenous malformation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Capillary malformation without arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acrodysostosis 2, with or without hormone resistance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acrodysostosis 2, with or without hormone resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypogonadotropic hypogonadism 13 with or without anosmia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypogonadotropic hypogonadism 13 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation, with or without seizures, ARX-related Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypogonadotropic hypogonadism 10 with or without anosmia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypogonadotropic hypogonadism 10 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short-rib thoracic dysplasia 10 with or without polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adult i Blood Group with or without Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypogonadotropic hypogonadism 11 with or without anosmia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypogonadotropic hypogonadism 11 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
IFAP syndrome with or without BRESHECK syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short-rib thoracic dysplasia 3 with or without polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency 26 with or without neurologic abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency 26 with or without neurologic abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Goiter, multinodular 1, with or without sertoli-leydig cell tumors Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Goiter, multinodular 1, with or without sertoli-leydig cell tumors phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
H2AX complex, isolated from cells without IR exposure Gene Set From CORUM Protein Complexes proteins in the H2AX complex, isolated from cells without IR exposure protein complex from the CORUM Protein Complexes dataset.
DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy, Cystic, Without Megalencephaly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy, Cystic, Without Megalencephaly from the curated CTD Gene-Disease Associations dataset.
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.
Migraine without Aura Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Migraine without Aura from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS from the curated CTD Gene-Disease Associations dataset.
Bronchiectasis With Or Without Elevated Sweat Chloride 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 1 from the curated CTD Gene-Disease Associations dataset.
Bronchiectasis With Or Without Elevated Sweat Chloride 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 2 from the curated CTD Gene-Disease Associations dataset.
Bronchiectasis With Or Without Elevated Sweat Chloride 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 3 from the curated CTD Gene-Disease Associations dataset.
Immunodeficiency without anhidrotic ectodermal dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency without anhidrotic ectodermal dysplasia from the curated CTD Gene-Disease Associations dataset.
HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.
Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE from the curated CTD Gene-Disease Associations dataset.
Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement from the curated CTD Gene-Disease Associations dataset.
MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) from the curated CTD Gene-Disease Associations dataset.
Metaphyseal Dysplasia without Hypotrichosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Metaphyseal Dysplasia without Hypotrichosis from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.
ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.
PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.
Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.
THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA from the curated CTD Gene-Disease Associations dataset.
Nonmedullary thyroid carcinoma, with or without cell oxyphilia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nonmedullary thyroid carcinoma, with or without cell oxyphilia from the curated CTD Gene-Disease Associations dataset.
SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset.
Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia from the curated CTD Gene-Disease Associations dataset.
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.
Migraine without Aura Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Migraine without Aura in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
migraine without aura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease migraine without aura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cleft lip with cleft palate; cleft lip without cleft palate; cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
salmeterol with or without fluticasone propionate Gene Set From GAD Gene-Disease Associations genes associated with the disease salmeterol with or without fluticasone propionate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine disorders; migraine with aura; migraine without aura; tension-type headache Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders; migraine with aura; migraine without aura; tension-type headache in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip with or without cleft palate; cleft palate, isolated Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip with or without cleft palate; cleft palate, isolated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip with cleft palate; cleft lip without cleft palate; cleft lip Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate; cleft lip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv; tuberculosis; cleft lip with cleft palate; cleft lip without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv; tuberculosis; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine without aura Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine with aura; migraine without aura Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine with aura; migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip with cleft palate; cleft lip without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip with or without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonsyndromic cleft lipor without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease nonsyndromic cleft lipor without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine with and without aura Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine with and without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip without cleft palate; cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip without cleft palate; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
migraine disorders; migraine with aura; migraine without aura Gene Set From GAD Gene-Disease Associations genes associated with the disease migraine disorders; migraine with aura; migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital anomalies; cleft lip with or without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital anomalies; cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set From GAD Gene-Disease Associations genes associated with the disease thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonsyndromic cleft lip with or without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease nonsyndromic cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate Gene Set From GAD Gene-Disease Associations genes associated with the disease heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
without Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term without in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cell cycle comprising mitosis without cytokinesis Gene Set From GO Biological Process Annotations 2015 genes participating in the cell cycle comprising mitosis without cytokinesis biological process from the curated GO Biological Process Annotations 2015 dataset.
Migraine without aura Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Migraine without aura phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
migraine without aura Gene Set From GWASdb SNP-Disease Associations genes associated with the disease migraine without aura in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
migraine without aura Gene Set From GWASdb SNP-Phenotype Associations genes associated with the migraine without aura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
focal seizures without impairment of consciousness or awareness Gene Set From HPO Gene-Disease Associations genes associated with the focal seizures without impairment of consciousness or awareness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
migraine without aura Gene Set From HPO Gene-Disease Associations genes associated with the migraine without aura phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Migraine without Aura Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Migraine without Aura phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, progressive myoclonic 3, with or without intracellular inclusions Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypogonadotropic hypogonadism 15 with or without anosmia} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypogonadotropic hypogonadism 15 with or without anosmia} phenotype from the curated OMIM Gene-Disease Associations dataset.
spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 10 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
brain small vessel disease with or without ocular anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the brain small vessel disease with or without ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
paragangliomas 1, with or without deafness Gene Set From OMIM Gene-Disease Associations genes associated with the paragangliomas 1, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
metaphyseal dysplasia without hypotrichosis Gene Set From OMIM Gene-Disease Associations genes associated with the metaphyseal dysplasia without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 4 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
central hypoventilation syndrome, congenital, with or without hirschsprung disease Gene Set From OMIM Gene-Disease Associations genes associated with the central hypoventilation syndrome, congenital, with or without hirschsprung disease phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 14 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 14 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
waardenburg syndrome, type 2e, with or without neurologic involvement Gene Set From OMIM Gene-Disease Associations genes associated with the waardenburg syndrome, type 2e, with or without neurologic involvement phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly 2, primary, autosomal recessive, with or without cortical malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly 2, primary, autosomal recessive, with or without cortical malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
cognitive impairment with or without cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the cognitive impairment with or without cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 6 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 10 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 10 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 3 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 3 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine without aura, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine without aura, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 8 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 8 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
leukemia, megakaryoblastic, with or without down syndrome, somatic Gene Set From OMIM Gene-Disease Associations genes associated with the leukemia, megakaryoblastic, with or without down syndrome, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
antley-bixler syndrome without genital anomalies or disordered steroidogenesis Gene Set From OMIM Gene-Disease Associations genes associated with the antley-bixler syndrome without genital anomalies or disordered steroidogenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 5 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 5 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 7 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
?microtia with or without hearing impairment (ad) Gene Set From OMIM Gene-Disease Associations genes associated with the ?microtia with or without hearing impairment (ad) phenotype from the curated OMIM Gene-Disease Associations dataset.
anemia, x-linked, with/without neutropenia and/or platelet abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the anemia, x-linked, with/without neutropenia and/or platelet abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 11 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 11 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 18 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 18 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
{bronchiectasis with or without elevated sweat chloride 1, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {bronchiectasis with or without elevated sweat chloride 1, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine, with or without aura, susceptibility to, 12} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine, with or without aura, susceptibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.
?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness Gene Set From OMIM Gene-Disease Associations genes associated with the retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 11 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
?testicular anomalies with or without congenital heart disease Gene Set From OMIM Gene-Disease Associations genes associated with the ?testicular anomalies with or without congenital heart disease phenotype from the curated OMIM Gene-Disease Associations dataset.
dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema Gene Set From OMIM Gene-Disease Associations genes associated with the dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema phenotype from the curated OMIM Gene-Disease Associations dataset.
hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 2 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 2 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
bronchiectasis with or without elevated sweat chloride 1 Gene Set From OMIM Gene-Disease Associations genes associated with the bronchiectasis with or without elevated sweat chloride 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
bronchiectasis with or without elevated sweat chloride 2 Gene Set From OMIM Gene-Disease Associations genes associated with the bronchiectasis with or without elevated sweat chloride 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
bronchiectasis with or without elevated sweat chloride 3 Gene Set From OMIM Gene-Disease Associations genes associated with the bronchiectasis with or without elevated sweat chloride 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis Gene Set From OMIM Gene-Disease Associations genes associated with the foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
amyotrophic lateral sclerosis 6, autosomal recessive, with or without frontotemporal dementia Gene Set From OMIM Gene-Disease Associations genes associated with the amyotrophic lateral sclerosis 6, autosomal recessive, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.
acrodysostosis 1, with or without hormone resistance Gene Set From OMIM Gene-Disease Associations genes associated with the acrodysostosis 1, with or without hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 20 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 20 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
?hypogonadotropic hypogonadism 13 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the ?hypogonadotropic hypogonadism 13 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism Gene Set From OMIM Gene-Disease Associations genes associated with the leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.
pulmonary hypertension, familial primary, 1, with or without hht Gene Set From OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, familial primary, 1, with or without hht phenotype from the curated OMIM Gene-Disease Associations dataset.
?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
woolly hair, autosomal recessive 1, with or without hypotrichosis Gene Set From OMIM Gene-Disease Associations genes associated with the woolly hair, autosomal recessive 1, with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 4 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 4 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
dementia, frontotemporal, with or without parkinsonism Gene Set From OMIM Gene-Disease Associations genes associated with the dementia, frontotemporal, with or without parkinsonism phenotype from the curated OMIM Gene-Disease Associations dataset.
leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism Gene Set From OMIM Gene-Disease Associations genes associated with the leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 9 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 9 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 9 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine without aura, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine without aura, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
left ventricular noncompaction 1, with or without congenital heart defects Gene Set From OMIM Gene-Disease Associations genes associated with the left ventricular noncompaction 1, with or without congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.
tooth agenesis, selective, 1, with or without orofacial cleft Gene Set From OMIM Gene-Disease Associations genes associated with the tooth agenesis, selective, 1, with or without orofacial cleft phenotype from the curated OMIM Gene-Disease Associations dataset.
{pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
?hypogonadotropic hypogonadism 12 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the ?hypogonadotropic hypogonadism 12 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set From OMIM Gene-Disease Associations genes associated with the polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 6 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 6 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
ciliary dyskinesia, primary, 9, with or without situs inversus Gene Set From OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 9, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.
clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract, pulverulent or cerulean, with or without microcornea Gene Set From OMIM Gene-Disease Associations genes associated with the cataract, pulverulent or cerulean, with or without microcornea phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombocytopenia, x-linked, with or without dyserythropoietic anemia Gene Set From OMIM Gene-Disease Associations genes associated with the thrombocytopenia, x-linked, with or without dyserythropoietic anemia phenotype from the curated OMIM Gene-Disease Associations dataset.
gastric cancer, familial diffuse, with or without cleft lip and/or palate Gene Set From OMIM Gene-Disease Associations genes associated with the gastric cancer, familial diffuse, with or without cleft lip and/or palate phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 3 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
retinitis pigmentosa with or without situs inversus Gene Set From OMIM Gene-Disease Associations genes associated with the retinitis pigmentosa with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 1 with or without anosmia (kallmann syndrome 1) Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 1 with or without anosmia (kallmann syndrome 1) phenotype from the curated OMIM Gene-Disease Associations dataset.
ciliary dyskinesia, primary, 7, with or without situs inversus Gene Set From OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 7, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.
gyrate atrophy of choroid and retina with or without ornithinemia Gene Set From OMIM Gene-Disease Associations genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 19 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 19 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine with or without aura, susceptibility to, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine with or without aura, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, with or without nystagmus Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, with or without nystagmus phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, neurosensory, without vestibular involvement, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, neurosensory, without vestibular involvement, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
amyotrophic lateral sclerosis 14, with or without frontotemporal dementia Gene Set From OMIM Gene-Disease Associations genes associated with the amyotrophic lateral sclerosis 14, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.
adult i phenotype without cataract Gene Set From OMIM Gene-Disease Associations genes associated with the adult i phenotype without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy, cystic, without megalencephaly Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy, cystic, without megalencephaly phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine with or without aura, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine with or without aura, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 8 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
branchiootorenal syndrome 1, with or without cataracts Gene Set From OMIM Gene-Disease Associations genes associated with the branchiootorenal syndrome 1, with or without cataracts phenotype from the curated OMIM Gene-Disease Associations dataset.
mcleod syndrome with or without chronic granulomatous disease Gene Set From OMIM Gene-Disease Associations genes associated with the mcleod syndrome with or without chronic granulomatous disease phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine with or without aura, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine with or without aura, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
ciliary dyskinesia, primary, 1, with or without situs inversus Gene Set From OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 1, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.
mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set From OMIM Gene-Disease Associations genes associated with the mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine, with or without aura, susceptibility to, 13} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine, with or without aura, susceptibility to, 13} phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypogonadotropic hypogonadism 16 with or without anosmia} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypogonadotropic hypogonadism 16 with or without anosmia} phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 7, with or without av conduction defects Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.
bifid nose with or without anorectal and renal anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the bifid nose with or without anorectal and renal anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
androgen insensitivity, partial, with or without breast cancer Gene Set From OMIM Gene-Disease Associations genes associated with the androgen insensitivity, partial, with or without breast cancer phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 17 with or without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 17 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, progressive, with or without lipodystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, progressive, with or without lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 2 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
woolly hair, autosomal recessive 2 with or without hypotrichosis Gene Set From OMIM Gene-Disease Associations genes associated with the woolly hair, autosomal recessive 2 with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.
ifap syndrome with or without bresheck syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
hypertrichosis terminalis, generalized, with or without gingival hyperplasia Gene Set From OMIM Gene-Disease Associations genes associated with the hypertrichosis terminalis, generalized, with or without gingival hyperplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
immunodeficiency 16, with or without neurologic abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency 16, with or without neurologic abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
short-rib thoracic dysplasia 5 with or without polydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine with or without aura, susceptibility to Gene Set From OMIM Gene-Disease Associations genes associated with the migraine with or without aura, susceptibility to phenotype from the curated OMIM Gene-Disease Associations dataset.
ciliary dyskinesia, primary, 3, with or without situs inversus Gene Set From OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 3, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.
coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
acrodysostosis 2, with or without hormone resistance Gene Set From OMIM Gene-Disease Associations genes associated with the acrodysostosis 2, with or without hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperproinsulinemia, familial, with or without diabetes Gene Set From OMIM Gene-Disease Associations genes associated with the hyperproinsulinemia, familial, with or without diabetes phenotype from the curated OMIM Gene-Disease Associations dataset.
left ventricular noncompaction 3, with or without dilated cardiomyopathy Gene Set From OMIM Gene-Disease Associations genes associated with the left ventricular noncompaction 3, with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.
hypogonadotropic hypogonadism 7 without anosmia Gene Set From OMIM Gene-Disease Associations genes associated with the hypogonadotropic hypogonadism 7 without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.
anterior segment anomalies with or without cataract Gene Set From OMIM Gene-Disease Associations genes associated with the anterior segment anomalies with or without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, dopa-responsive, with or without hyperphenylalaninemia Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, dopa-responsive, with or without hyperphenylalaninemia phenotype from the curated OMIM Gene-Disease Associations dataset.
sweat chloride elevation without cf Gene Set From OMIM Gene-Disease Associations genes associated with the sweat chloride elevation without cf phenotype from the curated OMIM Gene-Disease Associations dataset.
amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set From OMIM Gene-Disease Associations genes associated with the amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.
?cardiac conduction disease with or without dilated cardiomyopathy Gene Set From OMIM Gene-Disease Associations genes associated with the ?cardiac conduction disease with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
amyotrophic lateral sclerosis 10, with or without ftd Gene Set From OMIM Gene-Disease Associations genes associated with the amyotrophic lateral sclerosis 10, with or without ftd phenotype from the curated OMIM Gene-Disease Associations dataset.
goiter, multinodular 1, with or without sertoli-leydig cell tumors Gene Set From OMIM Gene-Disease Associations genes associated with the goiter, multinodular 1, with or without sertoli-leydig cell tumors phenotype from the curated OMIM Gene-Disease Associations dataset.
Progressive Cone Dystrophy (Without Rod Involvement) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy (Without Rod Involvement) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cleft Lip With Or Without Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cleft Lip With Or Without Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonmedullary Thyroid Carcinoma, With Or Without Cell Oxyphilia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonmedullary Thyroid Carcinoma, With Or Without Cell Oxyphilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Respiratory Failure Without Hypercapnia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Respiratory Failure Without Hypercapnia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dentinogenesis Imperfecta Without Osteogenesis Imperfecta Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dentinogenesis Imperfecta Without Osteogenesis Imperfecta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyposis Of Gastric Fundus Without Polyposis Coli Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyposis Of Gastric Fundus Without Polyposis Coli in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Esophageal Atresia With Or Without Tracheoesophageal Fistula Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Atresia With Or Without Tracheoesophageal Fistula in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
2P21 Microdeletion Syndrome Without Cystinuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 2P21 Microdeletion Syndrome Without Cystinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chagas' Disease Without Mention Of Organ Involvement Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chagas' Disease Without Mention Of Organ Involvement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dengue Without Warning Signs Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dengue Without Warning Signs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Acute Myeloid Leukemia Without Maturation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Acute Myeloid Leukemia Without Maturation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sweat Chloride Elevation Without Cystic Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sweat Chloride Elevation Without Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Cholecystitis Without Calculus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Cholecystitis Without Calculus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Segment Anomalies With Or Without Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Segment Anomalies With Or Without Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vacterl Association, X-Linked, With Or Without Hydrocephalus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vacterl Association, X-Linked, With Or Without Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bpes Without Ovarian Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bpes Without Ovarian Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Malnutrition Without Mention Of Light-For-Dates Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Malnutrition Without Mention Of Light-For-Dates in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anemia, X-Linked, With Or Without Neutropenia And/Or Platelet Abnormalities Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anemia, X-Linked, With Or Without Neutropenia And/Or Platelet Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Testicular Anomalies With Or Without Congenital Heart Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Testicular Anomalies With Or Without Congenital Heart Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Narcolepsy Without Cataplexy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Narcolepsy Without Cataplexy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microtia With Or Without Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microtia With Or Without Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microtia Without Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microtia Without Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hypothyroidism Without Goiter Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypothyroidism Without Goiter in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duane Retraction Syndrome 3 With Or Without Deafness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duane Retraction Syndrome 3 With Or Without Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Combined Immunodeficiency And Megaloblastic Anemia With Or Without Hyperhomocysteinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Combined Immunodeficiency And Megaloblastic Anemia With Or Without Hyperhomocysteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brain Malformations With Or Without Urinary Tract Defects Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brain Malformations With Or Without Urinary Tract Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Capillary Malformation Without Arteriovenous Malformation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Capillary Malformation Without Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Metaphyseal Dysplasia With Maxillary Hypoplasia With Or Without Brachydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Metaphyseal Dysplasia With Maxillary Hypoplasia With Or Without Brachydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cognitive Impairment With Or Without Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cognitive Impairment With Or Without Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonsyndromic Cleft Lip With Or Without Cleft Palate Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonsyndromic Cleft Lip With Or Without Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Genetic Hyperferritinemia Without Iron Overload Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Genetic Hyperferritinemia Without Iron Overload in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cell cycle comprising mitosis without cytokinesis Gene Set From GO Biological Process Annotations 2023 genes participating in the cell cycle comprising mitosis without cytokinesis biological process from the curated GO Biological Process Annotations 2023 dataset.
cell cycle comprising mitosis without cytokinesis Gene Set From GO Biological Process Annotations 2025 genes participating in the cell cycle comprising mitosis without cytokinesis biological process from the curated GO Biological Process Annotations 2025 dataset.
short-rib thoracic dysplasia 9 with or without polydactyly Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease short-rib thoracic dysplasia 9 with or without polydactyly from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 22 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 22 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 6 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 6 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 9 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 9 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 12 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 12 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Migraine without aura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Migraine without aura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary autosomal recessive microcephaly 2 with or without cortical malformations Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary autosomal recessive microcephaly 2 with or without cortical malformations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 15 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 15 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 6 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 6 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acute myeloid leukemia without maturation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acute myeloid leukemia without maturation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 4 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 4 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked cleft palate with or without ankyloglossia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked cleft palate with or without ankyloglossia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental delay and seizures with or without movement abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental delay and seizures with or without movement abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 10 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 10 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 23 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 23 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 2 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 2 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 14 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 14 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial progressive hyperpigmentation with or without hypopigmentation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial progressive hyperpigmentation with or without hypopigmentation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 18 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 18 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 3 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 3 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 5 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 5 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 7 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 7 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 8 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 8 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 11 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 11 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 13 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 13 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
short-rib thoracic dysplasia 7 with or without polydactyly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease short-rib thoracic dysplasia 7 with or without polydactyly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 16 with or without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 16 with or without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypogonadotropic hypogonadism 24 without anosmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypogonadotropic hypogonadism 24 without anosmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Antley-Bixler syndrome without disordered steroidogenesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Antley-Bixler syndrome without disordered steroidogenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Restless legs syndrome in migraine without aura Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Restless legs syndrome in migraine without aura phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Migraine without aura Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Migraine without aura phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Nonsyndromic cleft lip with or without cleft palate Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nonsyndromic cleft lip with or without cleft palate phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip with or without cleft palate x maternal periconceptional alcohol use interaction (parent of origin effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate x maternal periconceptional alcohol use interaction (parent of origin effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip with or without cleft palate x maternal periconceptional smoking interaction (parent of origin effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate x maternal periconceptional smoking interaction (parent of origin effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip with or without cleft palate x maternal periconceptional vitamin use interaction (parent of origin effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate x maternal periconceptional vitamin use interaction (parent of origin effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Acute anterior uveitis (with or without ankylosing spondylitis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute anterior uveitis (with or without ankylosing spondylitis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Nonsyndromic cleft lip with or without cleft palate x sex interaction (2df test) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nonsyndromic cleft lip with or without cleft palate x sex interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Pulmonary arterial hypertension (without BMPR2 mutations) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulmonary arterial hypertension (without BMPR2 mutations) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip with or without cleft palate (maternal periconceptional vitamin use interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate (maternal periconceptional vitamin use interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cleft lip with or without cleft palate (maternal periconceptional alcohol intake interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cleft lip with or without cleft palate (maternal periconceptional alcohol intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bicuspid aortic valve without aortic dilation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bicuspid aortic valve without aortic dilation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sarcoidosis (non-Lofgren's syndrome without extrapulmonary manifestations) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sarcoidosis (non-Lofgren's syndrome without extrapulmonary manifestations) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Spontaneous preterm birth without premature rupture of membranes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spontaneous preterm birth without premature rupture of membranes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Peroxisome biogenesis disorder 9B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 9B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 3A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 3A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia-telangiectasia-like disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 8B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 8B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 8A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 8A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisomal fatty acyl-coa reductase 1 disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisomal fatty acyl-coa reductase 1 disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 7B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 7A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 7A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rett's disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rett's disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nijmegen breakage syndrome-like disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nijmegen breakage syndrome-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Platelet-type bleeding disorder 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Platelet-type bleeding disorder 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Platelet-type bleeding disorder 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Platelet-type bleeding disorder 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Platelet-type bleeding disorder 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Platelet-type bleeding disorder 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Platelet-type bleeding disorder 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Platelet-type bleeding disorder 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1s Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2k Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2k phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1Q Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1P Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1H Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1N Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1v Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1v phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia-telangiectasia-like disorder 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia-like disorder 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial platelet disorder with associated myeloid malignancy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial platelet disorder with associated myeloid malignancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type Ix Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type Ix phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 4B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 5A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 5A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 5B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 5B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1K Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1O Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1G Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1y Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1y phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1u Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1u phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1t Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1t phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 11A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 11A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 11B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 11B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bleeding disorder, platelet-type, 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bleeding disorder, platelet-type, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bleeding disorder, platelet-type, 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bleeding disorder, platelet-type, 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Otopalatodigital spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Otopalatodigital spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 13A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 13A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Speech-language disorder 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Speech-language disorder 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 6A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 6A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 6B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 6B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic valve disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic valve disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stereotypic Movement Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stereotypic Movement Disorder from the curated CTD Gene-Disease Associations dataset.
Tobacco Use Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tobacco Use Disorder from the curated CTD Gene-Disease Associations dataset.
Speech-Sound Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Speech-Sound Disorder from the curated CTD Gene-Disease Associations dataset.
Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Platelet Disorder, Familial, with Associated Myeloid Malignancy from the curated CTD Gene-Disease Associations dataset.
Orthostatic Hypotensive Disorder, Streeten Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Orthostatic Hypotensive Disorder, Streeten Type from the curated CTD Gene-Disease Associations dataset.
Paroxysmal Extreme Pain Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Paroxysmal Extreme Pain Disorder from the curated CTD Gene-Disease Associations dataset.
Autistic Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Autistic Disorder from the curated CTD Gene-Disease Associations dataset.
Transient Myeloproliferative Disorder of Down Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Transient Myeloproliferative Disorder of Down Syndrome from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIF Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIF from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1A from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation, type 2C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation, type 2C from the curated CTD Gene-Disease Associations dataset.
NOG-Related-Symphalangism Spectrum Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NOG-Related-Symphalangism Spectrum Disorder from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2D from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi from the curated CTD Gene-Disease Associations dataset.
Conduct Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Conduct Disorder from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1G from the curated CTD Gene-Disease Associations dataset.
Pigmentary Disorder, Reticulate, with Systemic Manifestations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pigmentary Disorder, Reticulate, with Systemic Manifestations from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder of Glycosylation, Type Io Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder of Glycosylation, Type Io from the curated CTD Gene-Disease Associations dataset.
Bleeding Disorder, East Texas Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bleeding Disorder, East Texas Type from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type Im Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type Im from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type In Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type In from the curated CTD Gene-Disease Associations dataset.
Bipolar Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bipolar Disorder from the curated CTD Gene-Disease Associations dataset.
ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 from the curated CTD Gene-Disease Associations dataset.
PEROXISOME BIOGENESIS DISORDER 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PEROXISOME BIOGENESIS DISORDER 2B from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1H from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 8 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 9 from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1J from the curated CTD Gene-Disease Associations dataset.
Obsessive-Compulsive Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Obsessive-Compulsive Disorder from the curated CTD Gene-Disease Associations dataset.
Nijmegen Breakage Syndrome-Like Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nijmegen Breakage Syndrome-Like Disorder from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1B from the curated CTD Gene-Disease Associations dataset.
REM Sleep Behavior Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease REM Sleep Behavior Disorder from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2A from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2E from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip from the curated CTD Gene-Disease Associations dataset.
Depressive Disorder, Major Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Depressive Disorder, Major from the curated CTD Gene-Disease Associations dataset.
Antisocial Personality Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Antisocial Personality Disorder from the curated CTD Gene-Disease Associations dataset.
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency from the curated CTD Gene-Disease Associations dataset.
Myeloproliferative Disorder, Chronic, with Eosinophilia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myeloproliferative Disorder, Chronic, with Eosinophilia from the curated CTD Gene-Disease Associations dataset.
BLEEDING DISORDER, PLATELET-TYPE, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BLEEDING DISORDER, PLATELET-TYPE, 8 from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1F from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj from the curated CTD Gene-Disease Associations dataset.
Major Depressive Disorder 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Depressive Disorder 1 from the curated CTD Gene-Disease Associations dataset.
Major Depressive Disorder 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Depressive Disorder 2 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 4 from the curated CTD Gene-Disease Associations dataset.
Attention Deficit Disorder with Hyperactivity Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Attention Deficit Disorder with Hyperactivity from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type II from the curated CTD Gene-Disease Associations dataset.
NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1K Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1K from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1L Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1L from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1C from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1E from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1D from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation, type 2G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation, type 2G from the curated CTD Gene-Disease Associations dataset.
Depressive Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Depressive Disorder from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIH from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 2 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 3 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 1 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 6 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 7 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 5 from the curated CTD Gene-Disease Associations dataset.
SPEECH-LANGUAGE DISORDER 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPEECH-LANGUAGE DISORDER 1 from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIB from the curated CTD Gene-Disease Associations dataset.
Tobacco Use Disorder Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Tobacco Use Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Depressive Disorder, Major Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Depressive Disorder, Major in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Depressive Disorder Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Depressive Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Autistic Disorder Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Autistic Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Conduct Disorder Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Conduct Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Bipolar Disorder Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Bipolar Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Attention Deficit Disorder with Hyperactivity Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Attention Deficit Disorder with Hyperactivity in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
congenital disorder of glycosylation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital disorder of glycosylation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
carbohydrate metabolic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease carbohydrate metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cognitive disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cognitive disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
metal metabolism disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease metal metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
glycogen metabolism disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease glycogen metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
urea cycle disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease urea cycle disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
pervasive developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease pervasive developmental disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
physical disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease physical disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
specific developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease specific developmental disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
gamma-amino butyric acid metabolism disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease gamma-amino butyric acid metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
tic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease tic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
purine-pyrimidine metabolic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease purine-pyrimidine metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
sleep disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease sleep disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
bilirubin metabolic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bilirubin metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
amino acid metabolic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease amino acid metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
inherited metabolic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease inherited metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease developmental disorder of mental health from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
lipid metabolism disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease lipid metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
psychotic disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease psychotic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
sexual disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease sexual disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
cognitive disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease cognitive disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
mood disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease mood disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
conduct disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease conduct disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
substance-related disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease substance-related disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
physical disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease physical disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
impulse control disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease impulse control disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
specific developmental disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease specific developmental disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
attention deficit hyperactivity disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease attention deficit hyperactivity disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
inherited metabolic disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease inherited metabolic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
bipolar disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease bipolar disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
eating disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease eating disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
tic disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease tic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
sleep disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease sleep disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
autistic disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease autistic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
autism spectrum disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease autism spectrum disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease developmental disorder of mental health in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
lipid metabolism disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease lipid metabolism disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
pervasive developmental disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease pervasive developmental disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
personality disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease personality disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
anxiety disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease anxiety disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
stereotypic movement disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease stereotypic movement disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bipolar disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bipolar disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital disorder of glycosylation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital disorder of glycosylation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
body dysmorphic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease body dysmorphic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital disorder of glycosylation type ii Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital disorder of glycosylation type ii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
somatization disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease somatization disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cyclothymic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cyclothymic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
paraphilia disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease paraphilia disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lipid metabolism disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lipid metabolism disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
histrionic personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease histrionic personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
psychotic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease psychotic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
schizotypal personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease schizotypal personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sexual disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sexual disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
carbohydrate metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease carbohydrate metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vitamin metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vitamin metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mood disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mood disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neurotic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neurotic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
conduct disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease conduct disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
post-traumatic stress disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease post-traumatic stress disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic tic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic tic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
urea cycle disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urea cycle disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
avoidant personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease avoidant personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pervasive developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pervasive developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen metabolism disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen metabolism disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dysthymic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dysthymic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
periodic limb movement disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease periodic limb movement disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
combat disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease combat disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
expressive language disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease expressive language disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gender identity disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gender identity disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autism spectrum disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autism spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
purine-pyrimidine metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease purine-pyrimidine metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
amino acid metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease amino acid metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
paranoid personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease paranoid personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
schizoaffective disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease schizoaffective disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sleep disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sleep disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
borderline personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease borderline personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
obsessive-compulsive disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease obsessive-compulsive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
articulation disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease articulation disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anxiety disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anxiety disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
psychosexual disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease psychosexual disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
antisocial personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease antisocial personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dependent personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dependent personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
somatoform disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease somatoform disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
steroid inherited metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease steroid inherited metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
generalized anxiety disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease generalized anxiety disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
metal metabolism disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease metal metabolism disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dissociative disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dissociative disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
schizoid personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease schizoid personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fetal alcohol spectrum disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal alcohol spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
substance-related disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease substance-related disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
physical disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease physical disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
communication disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease communication disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alcohol-induced mental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intermittent explosive disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intermittent explosive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
speech disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease speech disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autistic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autistic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
attention deficit hyperactivity disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease attention deficit hyperactivity disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bipolar i disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bipolar i disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
inherited metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inherited metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
obsessive-compulsive personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease obsessive-compulsive personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
schizophreniform disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease schizophreniform disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alcohol-related neurodevelopmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-related neurodevelopmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease developmental disorder of mental health in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
amnestic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease amnestic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
reading disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease reading disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
writing disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease writing disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bilirubin metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bilirubin metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
language disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease language disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cognitive disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cognitive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
seasonal affective disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease seasonal affective disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
developmental coordination disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease developmental coordination disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
eating disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eating disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
rumination disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease rumination disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
withdrawal disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease withdrawal disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
impulse control disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease impulse control disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
delusional disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease delusional disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
specific developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease specific developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
drug-induced mental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease drug-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
major depressive disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease major depressive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
acute stress disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acute stress disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hypoactive sexual desire disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypoactive sexual desire disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pain disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pain disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
phobic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease phobic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
narcissistic personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease narcissistic personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital disorder of glycosylation type i Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital disorder of glycosylation type i in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
adjustment disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adjustment disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gamma-amino butyric acid metabolism disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gamma-amino butyric acid metabolism disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
factitious disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease factitious disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atypical depressive disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atypical depressive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
separation anxiety disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease separation anxiety disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
obsessive compulsive disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease obsessive compulsive disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressive disorder, major; alcoholism Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; depressive disorder, major Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; depressive disorder, major in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit hyperactivity disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; alcoholism; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; alcoholism; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease mental disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; bipolar disorder; psychoses Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; bipolar disorder; psychoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; seasonal affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; seasonal affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung neoplasms; neoplasm of lung ; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease lung neoplasms; neoplasm of lung ; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
conduct disorder (interaction) Gene Set From GAD Gene-Disease Associations genes associated with the disease conduct disorder (interaction) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obsessive-compulsive disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease obsessive-compulsive disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety disorder; blood pressure, arterial; memory impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety disorder; blood pressure, arterial; memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
visual disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease visual disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
posttraumatic stress disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease posttraumatic stress disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercholesterolemia; h. pylori infection; coagulation disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercholesterolemia; h. pylori infection; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adhd ; attention-deficit hyperactivity disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease adhd ; attention-deficit hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
major depressive disorder (broad) Gene Set From GAD Gene-Disease Associations genes associated with the disease major depressive disorder (broad) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
post-traumatic stress disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease post-traumatic stress disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar and unipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar and unipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar schizoaffective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar schizoaffective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amino acid disorder, nos; amino acid metabolism, inborn errors; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease amino acid disorder, nos; amino acid metabolism, inborn errors; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy complications; tic disorder; tic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy complications; tic disorder; tic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; head and neck neoplasms; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; anxiety disorder; depression; psychoses; aggressive behavior Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; anxiety disorder; depression; psychoses; aggressive behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antisocial behavior conduct disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease antisocial behavior conduct disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy loss, recurrent; coagulation disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar disorder; mania, antidepressant-induced Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar disorder; mania, antidepressant-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
porphyrias; porphyrin disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease porphyrias; porphyrin disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mood disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease mood disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
opioid-related disorders; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease opioid-related disorders; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; autism; alcoholism; attention deficit hyperactivity disorder; cocaine abuse; psychosis, puerperal Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; autism; alcoholism; attention deficit hyperactivity disorder; cocaine abuse; psychosis, puerperal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety disorder; alcoholism; depression; narcolepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety disorder; alcoholism; depression; narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
seasonal affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease seasonal affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention-deficit/hyperactivity disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease attention-deficit/hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
major depressive disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease major depressive disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obsessive- compulsive disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease obsessive- compulsive disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia ; depression ; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia ; depression ; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; squamous cell carcinoma; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; squamous cell carcinoma; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety disorder; alcoholism Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety disorder; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eating disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease eating disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of the optic nerve; glaucoma, open-angle; optic nerve diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit hyperactivity disorder-like phenotype Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit hyperactivity disorder-like phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar affective disorder. Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar affective disorder. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit hyperactivity disorder; reading disability Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit hyperactivity disorder; reading disability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety disorder; depression Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety disorder; depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
impulse control disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease impulse control disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autistic disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease autistic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mood disorder. Gene Set From GAD Gene-Disease Associations genes associated with the disease mood disorder. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety disorder; alcohol abuse Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety disorder; alcohol abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressive disorder, major; nausea Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; nausea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sleep disorders; depressive disorder, major Gene Set From GAD Gene-Disease Associations genes associated with the disease sleep disorders; depressive disorder, major in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tic disorder; tic disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease tic disorder; tic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behavioral disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease behavioral disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coagulation disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; bipolar disorder; suicide; anorexia nervosa; bulimia; substance abuse Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; bipolar disorder; suicide; anorexia nervosa; bulimia; substance abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
quebec platelet disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease quebec platelet disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; mouth neoplasms; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; mouth neoplasms; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar disorder; affective psychoses Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar disorder; affective psychoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; delusional disorder; aggressive behavior Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; delusional disorder; aggressive behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; mood disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; mood disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol abuse; impulse control disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol abuse; impulse control disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
binge eating disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease binge eating disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperkinetic disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperkinetic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
peroxisome-biogenesis disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease peroxisome-biogenesis disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention-deficit hyperactivity disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease attention-deficit hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adhd and conduct disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease adhd and conduct disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrence; substance withdrawal syndrome; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrence; substance withdrawal syndrome; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; schizoaffective disorder; weight gain Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; schizoaffective disorder; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
posttraumatic stress disorder. Gene Set From GAD Gene-Disease Associations genes associated with the disease posttraumatic stress disorder. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
substance withdrawal syndrome; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease substance withdrawal syndrome; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes, type 2; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar disorder ; mood disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar disorder ; mood disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit hyperactivity disorder symptoms (interaction) Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit hyperactivity disorder symptoms (interaction) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ulcer, gastric; repaglinide pharmacology; coagulation disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease ulcer, gastric; repaglinide pharmacology; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar disorder; depression Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar disorder; depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
borderline personality disorder and aggression Gene Set From GAD Gene-Disease Associations genes associated with the disease borderline personality disorder and aggression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinson's disease; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinson's disease; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung neoplasms; neoplasm of lung (disorder); occupational diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease lung neoplasms; neoplasm of lung (disorder); occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressive disorder, major; suicide Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; suicide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adhd ; attention deficit hyperactivity disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease adhd ; attention deficit hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delusional disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease delusional disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult adhd ; attention deficit hyperactivity disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease adult adhd ; attention deficit hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
conduct disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease conduct disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amino acid disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease amino acid disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; cocaine-related disorders; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; cocaine-related disorders; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
transient myeloproliferative disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease transient myeloproliferative disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia and bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia and bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multisomatoform disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease multisomatoform disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; marijuana abuse; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; marijuana abuse; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
monosymptomatic psychotic disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease monosymptomatic psychotic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus (disorder) Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus (disorder) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressive disorder, major Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorder, major in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autism spectrum disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease autism spectrum disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
methamphetamine psychotic disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease methamphetamine psychotic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes, gestational; gestational diabetes mellitus (disorder) Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, gestational; gestational diabetes mellitus (disorder) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adhd ; post-traumatic stress disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease adhd ; post-traumatic stress disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressive disorder, major; phobia Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; phobia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adhd ; oppositional defiant disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease adhd ; oppositional defiant disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; attention deficit hyperactivity disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; attention deficit hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; schizoaffective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; schizoaffective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar i disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar i disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia ; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia ; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressive disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amino acid disorder, nos; amino acid metabolism, inborn errors Gene Set From GAD Gene-Disease Associations genes associated with the disease amino acid disorder, nos; amino acid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperkinetic conduct disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperkinetic conduct disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mouth neoplasms; pharyngeal neoplasms; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease mouth neoplasms; pharyngeal neoplasms; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of muscle, unspec; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit hyperactivity disorder (time to onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit hyperactivity disorder (time to onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, transitional cell; tobacco use disorder; urinary bladder neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, transitional cell; tobacco use disorder; urinary bladder neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depression ; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease depression ; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit disorder with hyperactivity Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit disorder with hyperactivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
borderline personality disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease borderline personality disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antisocial personality disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease antisocial personality disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autistic spectrum disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease autistic spectrum disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of muscle, unspec; hypercholesterolemia; muscular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; hypercholesterolemia; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuroblastoma; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease neuroblastoma; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term disorder in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Response to serotonin reuptake inhibitors in major depressive disorder (plasma drug and metabolite levels) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to serotonin reuptake inhibitors in major depressive disorder (plasma drug and metabolite levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asperger disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asperger disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bipolar I disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bipolar I disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Attention deficit hyperactivity disorder (hyperactivity-impulsivity symptoms) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Attention deficit hyperactivity disorder (hyperactivity-impulsivity symptoms) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Anxiety and major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Anxiety and major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Alcoholism (alcohol use disorder factor score) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Alcoholism (alcohol use disorder factor score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Temperament (bipolar disorder) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Temperament (bipolar disorder) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bipolar disorder (body mass index interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bipolar disorder (body mass index interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Conduct disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Conduct disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bipolar disorder and schizophrenia Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Attention deficit hyperactivity disorder symptoms (interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Attention deficit hyperactivity disorder symptoms (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Attention deficit hyperactivity disorder (inattention symptoms) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Attention deficit hyperactivity disorder (inattention symptoms) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Schizophrenia or bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Schizophrenia or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Schizophrenia, bipolar disorder and depression (combined) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Schizophrenia, bipolar disorder and depression (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Major depressive disorder (broad) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Major depressive disorder (broad) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Borderline personality disorder features Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Borderline personality disorder features phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Attention deficit hyperactivity disorder (combined symptoms) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Attention deficit hyperactivity disorder (combined symptoms) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bipolar disorder (age of onset and psychomotor symptoms) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bipolar disorder (age of onset and psychomotor symptoms) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Suicidal ideation in depression or bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Suicidal ideation in depression or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Suicide attempts in bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Suicide attempts in bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Post-traumatic stress disorder (asjusted for relatedness) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Post-traumatic stress disorder (asjusted for relatedness) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bipolar disorder (mood-incongruent) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bipolar disorder (mood-incongruent) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Conduct disorder (interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Conduct disorder (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Anxiety in major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Anxiety in major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Response to methylphenidate treatment in attention-deficit/hyperactivity disorder (blood pressure) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to methylphenidate treatment in attention-deficit/hyperactivity disorder (blood pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Attention deficit hyperactivity disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Attention deficit hyperactivity disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Post-traumatic stress disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Post-traumatic stress disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Suicide attempts in depression or bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Suicide attempts in depression or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Attention deficit hyperactivity disorder (time to onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Attention deficit hyperactivity disorder (time to onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Conduct disorder (symptom count) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Conduct disorder (symptom count) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
bilirubin metabolic disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease bilirubin metabolic disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
psychotic disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease psychotic disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
communication disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease communication disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
sexual disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease sexual disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
language disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease language disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
cognitive disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease cognitive disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
metal metabolism disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease metal metabolism disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
mood disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease mood disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
conduct disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease conduct disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
substance-related disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease substance-related disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
withdrawal disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease withdrawal disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
physical disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease physical disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
impulse control disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease impulse control disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
specific developmental disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease specific developmental disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
drug-induced mental disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease drug-induced mental disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
attention deficit hyperactivity disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease attention deficit hyperactivity disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
inherited metabolic disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease inherited metabolic disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
major depressive disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease major depressive disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
reading disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease reading disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
bipolar disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease bipolar disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
speech disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease speech disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
eating disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease eating disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
anxiety disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease anxiety disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
tic disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease tic disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
sleep disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease sleep disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
borderline personality disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease borderline personality disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
autistic disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease autistic disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
autism spectrum disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease autism spectrum disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
alcohol-induced mental disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease alcohol-induced mental disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
schizoaffective disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease schizoaffective disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
developmental disorder of mental health Gene Set From GWASdb SNP-Disease Associations genes associated with the disease developmental disorder of mental health in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
lipid metabolism disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease lipid metabolism disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
pervasive developmental disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease pervasive developmental disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
post-traumatic stress disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease post-traumatic stress disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
obsessive-compulsive disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease obsessive-compulsive disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
personality disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease personality disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
vitamin metabolic disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease vitamin metabolic disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
bipolar affective disorder Gene Set From GWASdb SNP-Phenotype Associations genes associated with the bipolar affective disorder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
myeloproliferative disorder Gene Set From GWASdb SNP-Phenotype Associations genes associated with the myeloproliferative disorder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
attention deficit hyperactivity disorder Gene Set From GWASdb SNP-Phenotype Associations genes associated with the attention deficit hyperactivity disorder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
borderline personality disorder Gene Set From GWASdb SNP-Phenotype Associations genes associated with the borderline personality disorder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
personality disorder Gene Set From GWASdb SNP-Phenotype Associations genes associated with the personality disorder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
progressive extrapyramidal movement disorder Gene Set From HPO Gene-Disease Associations genes associated with the progressive extrapyramidal movement disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lymphoproliferative disorder Gene Set From HPO Gene-Disease Associations genes associated with the lymphoproliferative disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bipolar affective disorder Gene Set From HPO Gene-Disease Associations genes associated with the bipolar affective disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
personality disorder Gene Set From HPO Gene-Disease Associations genes associated with the personality disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
attention deficit hyperactivity disorder Gene Set From HPO Gene-Disease Associations genes associated with the attention deficit hyperactivity disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive disorder Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
myeloproliferative disorder Gene Set From HPO Gene-Disease Associations genes associated with the myeloproliferative disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive disorder Gene Set From HPO Gene-Disease Associations genes associated with the progressive disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Tobacco Use Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Tobacco Use Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Autistic Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Autistic Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Reactive Attachment Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Reactive Attachment Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Dysthymic Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dysthymic Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Conduct Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Conduct Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Bipolar Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Bipolar Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Compulsive Personality Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Compulsive Personality Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Schizoid Personality Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Schizoid Personality Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Obsessive-Compulsive Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Obsessive-Compulsive Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Stereotypic Movement Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Stereotypic Movement Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
REM Sleep Behavior Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the REM Sleep Behavior Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Depressive Disorder, Major Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Depressive Disorder, Major phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Antisocial Personality Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Antisocial Personality Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Schizotypal Personality Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Schizotypal Personality Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Attention Deficit Disorder with Hyperactivity Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Attention Deficit Disorder with Hyperactivity phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Borderline Personality Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Borderline Personality Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Binge-Eating Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Binge-Eating Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Alcohol Amnestic Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Alcohol Amnestic Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Depressive Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Depressive Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cyclothymic Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cyclothymic Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Seasonal Affective Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Seasonal Affective Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Conversion Disorder Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Conversion Disorder phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
altered susceptibility to autoimmune disorder Gene Set From MPO Gene-Phenotype Associations gene mutations causing the altered susceptibility to autoimmune disorder phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to autoimmune disorder Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to autoimmune disorder phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to autoimmune disorder Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to autoimmune disorder phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{major affective disorder 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {major affective disorder 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
pigment disorder, reticulate Gene Set From OMIM Gene-Disease Associations genes associated with the pigment disorder, reticulate phenotype from the curated OMIM Gene-Disease Associations dataset.
{major depressive disorder, response to citalopram therapy in} Gene Set From OMIM Gene-Disease Associations genes associated with the {major depressive disorder, response to citalopram therapy in} phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ih Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ih phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ij Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ij phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ik Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ik phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type il Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type il phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type im Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type im phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ia Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ic Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type id Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type id phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ie Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ie phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type if Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type if phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ig Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ig phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iq Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iq phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type it Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type it phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iu Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iu phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iv Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 5a (zellweger) Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 5a (zellweger) phenotype from the curated OMIM Gene-Disease Associations dataset.
bleeding disorder due to p2rx1 defect Gene Set From OMIM Gene-Disease Associations genes associated with the bleeding disorder due to p2rx1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 13a (zellweger) Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 13a (zellweger) phenotype from the curated OMIM Gene-Disease Associations dataset.
{major affective disorder-8, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {major affective disorder-8, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{seasonal affective disorder, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {seasonal affective disorder, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
paroxysmal extreme pain disorder, 167400, Gene Set From OMIM Gene-Disease Associations genes associated with the paroxysmal extreme pain disorder, 167400, phenotype from the curated OMIM Gene-Disease Associations dataset.
?congenital disorder of glycosylation, type iw Gene Set From OMIM Gene-Disease Associations genes associated with the ?congenital disorder of glycosylation, type iw phenotype from the curated OMIM Gene-Disease Associations dataset.
?congenital disorder of glycosylation, type ix Gene Set From OMIM Gene-Disease Associations genes associated with the ?congenital disorder of glycosylation, type ix phenotype from the curated OMIM Gene-Disease Associations dataset.
?congenital disorder of glycosylation, type iy Gene Set From OMIM Gene-Disease Associations genes associated with the ?congenital disorder of glycosylation, type iy phenotype from the curated OMIM Gene-Disease Associations dataset.
{attention deficit-hyperactivity disorder, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {attention deficit-hyperactivity disorder, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
major affective disorder 4 Gene Set From OMIM Gene-Disease Associations genes associated with the major affective disorder 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
{attention deficit-hyperactivity disorder} Gene Set From OMIM Gene-Disease Associations genes associated with the {attention deficit-hyperactivity disorder} phenotype from the curated OMIM Gene-Disease Associations dataset.
?congenital disorder of glycosylation, type ir Gene Set From OMIM Gene-Disease Associations genes associated with the ?congenital disorder of glycosylation, type ir phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 2a (zellweger) Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 2a (zellweger) phenotype from the curated OMIM Gene-Disease Associations dataset.
hepatic failure, early onset, and neurologic disorder Gene Set From OMIM Gene-Disease Associations genes associated with the hepatic failure, early onset, and neurologic disorder phenotype from the curated OMIM Gene-Disease Associations dataset.
{major affective disorder 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {major affective disorder 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type in Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type in phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type io Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type io phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ip Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ip phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type is Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type is phenotype from the curated OMIM Gene-Disease Associations dataset.
{bleeding disorder, platelet-type, 13, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {bleeding disorder, platelet-type, 13, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
hartnup disorder Gene Set From OMIM Gene-Disease Associations genes associated with the hartnup disorder phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 11a (zellweger) Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 11a (zellweger) phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia-telangiectasia-like disorder Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia-telangiectasia-like disorder phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 3b Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 5b Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 5b phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 7b Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 7b phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 14b Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 14b phenotype from the curated OMIM Gene-Disease Associations dataset.
{major affective disorder-7, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {major affective disorder-7, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
giant platelet disorder, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the giant platelet disorder, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
{obsessive-compulsive disorder, protection against} Gene Set From OMIM Gene-Disease Associations genes associated with the {obsessive-compulsive disorder, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset.
{attention deficit-hyperactivity disorder, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {attention deficit-hyperactivity disorder, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
bleeding disorder, platelet-type, 16, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the bleeding disorder, platelet-type, 16, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
?ataxia-telangiectasia-like disorder Gene Set From OMIM Gene-Disease Associations genes associated with the ?ataxia-telangiectasia-like disorder phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 9b Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 9b phenotype from the curated OMIM Gene-Disease Associations dataset.
bleeding disorder, platelet-type, 17 Gene Set From OMIM Gene-Disease Associations genes associated with the bleeding disorder, platelet-type, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
bleeding disorder, platelet-type, 15 Gene Set From OMIM Gene-Disease Associations genes associated with the bleeding disorder, platelet-type, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
bleeding disorder, platelet-type, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the bleeding disorder, platelet-type, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 10a (zellweger) Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 10a (zellweger) phenotype from the curated OMIM Gene-Disease Associations dataset.
{schizoaffective disorder, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {schizoaffective disorder, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
speech-language disorder-1 Gene Set From OMIM Gene-Disease Associations genes associated with the speech-language disorder-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 11b Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 11b phenotype from the curated OMIM Gene-Disease Associations dataset.
quebec platelet disorder Gene Set From OMIM Gene-Disease Associations genes associated with the quebec platelet disorder phenotype from the curated OMIM Gene-Disease Associations dataset.
{?major affective disorder 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {?major affective disorder 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
bleeding disorder, platelet-type, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the bleeding disorder, platelet-type, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
nail disorder, nonsyndromic congenital, 3, (leukonychia) Gene Set From OMIM Gene-Disease Associations genes associated with the nail disorder, nonsyndromic congenital, 3, (leukonychia) phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 4a (zellweger) Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 4a (zellweger) phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 1a (zellweger) Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 1a (zellweger) phenotype from the curated OMIM Gene-Disease Associations dataset.
{major affective disorder 3, early onset} Gene Set From OMIM Gene-Disease Associations genes associated with the {major affective disorder 3, early onset} phenotype from the curated OMIM Gene-Disease Associations dataset.
platelet disorder, familial, with associated myeloid malignancy Gene Set From OMIM Gene-Disease Associations genes associated with the platelet disorder, familial, with associated myeloid malignancy phenotype from the curated OMIM Gene-Disease Associations dataset.
pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
nail disorder, nonsyndromic congenital, 10, (claw-shaped nails) Gene Set From OMIM Gene-Disease Associations genes associated with the nail disorder, nonsyndromic congenital, 10, (claw-shaped nails) phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 12a (zellweger) Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 12a (zellweger) phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 8a, (zellweger) Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 8a, (zellweger) phenotype from the curated OMIM Gene-Disease Associations dataset.
bleeding disorder, east texas type Gene Set From OMIM Gene-Disease Associations genes associated with the bleeding disorder, east texas type phenotype from the curated OMIM Gene-Disease Associations dataset.
{attention deficit-hyperactivity disorder, susceptibility to, 7} Gene Set From OMIM Gene-Disease Associations genes associated with the {attention deficit-hyperactivity disorder, susceptibility to, 7} phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iil Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iil phenotype from the curated OMIM Gene-Disease Associations dataset.
{attention deficit-hyperactivity disorder, susceptibility to, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {attention deficit-hyperactivity disorder, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
peroxisome biogenesis disorder 1b (nald/ird) Gene Set From OMIM Gene-Disease Associations genes associated with the peroxisome biogenesis disorder 1b (nald/ird) phenotype from the curated OMIM Gene-Disease Associations dataset.
nail disorder, nonsyndromic congenital, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the nail disorder, nonsyndromic congenital, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
{obsessive-compulsive disorder, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {obsessive-compulsive disorder, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
major depressive disorder 1 Gene Set From OMIM Gene-Disease Associations genes associated with the major depressive disorder 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
major depressive disorder 2 Gene Set From OMIM Gene-Disease Associations genes associated with the major depressive disorder 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
{obsessive-compulsive disorder} Gene Set From OMIM Gene-Disease Associations genes associated with the {obsessive-compulsive disorder} phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iij Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iij phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iik Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iik phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iih Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iih phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iim Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iim phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iib Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iic Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iia Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iia phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iif Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iif phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iig Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iig phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iid Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iid phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iie Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iie phenotype from the curated OMIM Gene-Disease Associations dataset.

Harmonizome 3.0

PAND1 Gene

PAND2 Gene

PAND3 Gene

OS4 Gene

TNFRSF10C Gene

CTEPH1 Gene

MGR3 Gene

MGR5 Gene

LILRA3 Gene

RIT2 Gene

RIT1 Gene

HTGH Gene

RPH3AL Gene

ANOP1 Gene

MGR12 Gene

SSD Gene

OHDS Gene

MAFD9 Gene

MAFD8 Gene

MAFD5 Gene

MAFD1 Gene

MAFD3 Gene

MDD2 Gene

MDD1 Gene

MAFD2 Gene

MAFD4 Gene

MAFD6 Gene

ADHD2 Gene

HDL3 Gene

BDET Gene

ADHD4 Gene

ADHD5 Gene

ADHD6 Gene

ADHD1 Gene

ADHD3 Gene

SCZD8 Gene

SCZD7 Gene

SCZD6 Gene

SCZD1 Gene

SCZD3 Gene

SCZD10 Gene

NDNC9 Gene

CLA3 Gene

SCZD2 Gene

PDR Gene

Panic Disorder Without Agoraphobia Gene Set

alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene Set

Panic Disorder With Agoraphobia Gene Set

anxiety disorder; depressive disorder, major; panic disorder Gene Set

major depressive disorder and panic disorder Gene Set

Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) Gene Set

Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) Gene Set

Anorexia nervosa, attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, or Tourette syndrome (pleiotropy) Gene Set

Panic Disorder Gene Set

Panic Disorder Gene Set

panic disorder Gene Set

panic disorder Gene Set

schizophrenia; panic disorder Gene Set

panic disorder; migraine Gene Set

panic disorder Gene Set

panic disorder and anxious personality Gene Set

Panic disorder Gene Set

panic disorder Gene Set

Panic Disorder Gene Set

panic disorder 3 Gene Set

panic disorder 2 Gene Set

panic disorder syndrome 1 Gene Set

{panic disorder, susceptibility to} Gene Set

Panic Disorder Gene Set

Panic disorder Gene Set

Panic disorder Gene Set

Agoraphobia Gene Set

agoraphobia Gene Set

agoraphobia Gene Set

agoraphobia Gene Set

Agoraphobia Gene Set

Agoraphobia Gene Set

Agoraphobia Gene Set

Agoraphobia Gene Set