Familial Aplasia Of The Vermis

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Results for "Familial Aplasia Of The Vermis": 53 genes, 1001 gene sets

Name
PTLAH Gene patella aplasia-hypoplasia
AAA1 Gene aortic aneurysm, familial* abdominal 1*
AAA3 Gene Aneurysm, familial* abdominal 3*
AAA2 Gene Aortic aneurysm, familial* abdominal 2*
AAA4 Gene Aortic aneurysm, familial* abdominal, 4*
ETL6 Gene Epilepsy, familial* temporal lobe, 6*
RCM2 Gene cardiomyopathy, familial* restrictive, 2*
ATFB8 Gene Atrial fibrillation, familial, 8
HNFJ3 Gene Hyperuricemic nephropathy, familial* juvenile, 3*
GPSC Gene gliosis, familial* progressive subcortical*
BHD Gene Beukes familial* hip dysplasia*
FAME4 Gene Epilepsy, familial* adult myoclonic, 4*
FAME3 Gene Epilepsy, familial* adult myoclonic, 3*
PFHB2 Gene Progressive familial* heart block, type II*
BFIS1 Gene benign familial* infantile convulsions*
HBN1 Gene Progressive familial* heart block, type I, locus 1*
ETL2 Gene epilepsy, familial* temporal lobe*
FHII Gene Hyperaldosteronism, familial, type II
FCMTE2 Gene familial cortical myoclonic tremor with epilepsy 2
FCMTE1 Gene familial cortical myoclonic tremor with epilepsy 1
GLM4 Gene Glioma, familial, 1
PSHK2 Gene Pseudohyperkalemia, familial, 2, due to red cell leak
VVS Gene Syncope, familial* vasovagal*
BFIS4 Gene Convulsions, benign familial* infantile, 4*
ATFB1 Gene Atrial fibrillation, familial* 1*
ATFB2 Gene familial atrial fibrillation 2
SXI2 Gene X inactivation, familial* skewed, 2*
BFIC2 Gene Benign familial* infantile convulsions-2*
FMTLE Gene Epilepsy, familial* mesial temporal lobe*
STUT3 Gene Stuttering, familial* persistent, 3*
STUT2 Gene Stuttering, familial* persistent 2*
STUT1 Gene Stuttering, familial* persistent 1*
STUT4 Gene Stuttering, familial* persistent, 4*
BRCD1 Gene cancer, familial, with in vitro radioresistance
MGR2 Gene Migraine, familial* typical, susceptibility to*
MGR3 Gene Migraine, familial, with or without aura, susceptibility to
MFT2 Gene Trichoepithelioma, multiple familial, 2
FEB9 Gene Febrile convulsions, familial, 9
ATFB5 Gene Atrial fibrillation, familial, 5
HTGS Gene Hypertriglyceridemia, familial
DIP Gene interstitial pneumonitis, desquamative, familial
CMH21 Gene Cardiomyopathy, familial* hypertrophic, 21*
CANDF1 Gene candidiasis, familial* 1*
ATPLS Gene antiphospholipid syndrome, familial
EOS Gene eosinophilia, familial
FEB10 Gene Febrile convulsions, familial, 10
LVNC2 Gene noncompaction of left ventricular myocardium, familial* isolated, autosomal dominant 2*
THCYTX Gene Thrombocytosis, familial* X-linked*
CMS1A1 Gene myasthenia gravis, familial* infantile, 1*
BPPV Gene vestibulopathy, familial
AAT2 Gene Aortic aneurysm, familial* thoracic 2*
AAT1 Gene Aortic aneurysm, familial* thoracic 1*
NKCD Gene Natural killer cell deficiency, familial* isolated*
Familial Aplasia Of The Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Aplasia Of The Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
aplasia of the inferior half of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the inferior half of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Aplasia/Hypoplasia Of The Cerebellar Vermis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Inferior Half Of The Cerebellar Vermis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Inferior Half Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
mantle zone of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in mantle zone of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
white matter of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in white matter of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cortex of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cortex of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
superficial stratum of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Folium-tuber vermis (VII), granular layer Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Folium-tuber vermis (VII), granular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Folium-tuber vermis (VII), molecular layer Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Folium-tuber vermis (VII), molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Folium-tuber vermis (VII) Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Folium-tuber vermis (VII) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
intermediate stratum of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in intermediate stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
periventricular stratum of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in periventricular stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cerebellar vermis Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar vermis relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
vermis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term vermis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
agenesis of cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the agenesis of cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dysgenesis of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the dysgenesis of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar vermis atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar vermis atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
inferior vermis hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the inferior vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar vermis hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
disorganization of the anterior cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the disorganization of the anterior cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
loss of purkinje cells in the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the loss of purkinje cells in the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal cerebellum posterior vermis morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum posterior vermis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum vermis lobule ii morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule ii morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cerebellum vermis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cerebellum vermis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cerebellum vermis lobule ix Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cerebellum vermis lobule ix phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum vermis lobule vi morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule vi morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum vermis lobule viii morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule viii morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum vermis lobule iii morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule iii morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum anterior vermis morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum anterior vermis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cerebellum vermis hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cerebellum vermis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum vermis lobule i morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule i morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum vermis lobule ix morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule ix morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum vermis morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum vermis lobule morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum vermis lobule vii morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule vii morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased anterior vermis size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased anterior vermis size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum vermis lobule v morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule v morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum vermis lobule iv morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule iv morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum vermis lobule x morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule x morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cerebellum vermis lobule viii Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cerebellum vermis lobule viii phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Dysgenesis Of The Cerebellar Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysgenesis Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Cerebellar Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Absence Of Cerebellar Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Absence Of Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Vermis Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Vermis Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Loss Of Purkinje Cells In The Cerebellar Vermis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Purkinje Cells In The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Vermis Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Vermis Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Inferior Vermis Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Inferior Vermis Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Disorganization Of The Anterior Cerebellar Vermis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disorganization Of The Anterior Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vermis Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vermis Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
abnormal cerebellum vermis morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cerebellum vermis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebellum vermis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum vermis lobule morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis lobule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum vermis lobule II morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis lobule II morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum vermis lobule III morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis lobule III morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum vermis lobule IV morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis lobule IV morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum vermis lobule V morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis lobule V morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum vermis lobule VI morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis lobule VI morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum vermis lobule VII morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis lobule VII morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum anterior vermis morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum anterior vermis morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cerebellum vermis lobule VIII Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebellum vermis lobule VIII phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cerebellum vermis lobule IX Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebellum vermis lobule IX phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cerebellum vermis hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebellum vermis hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased anterior vermis size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased anterior vermis size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum posterior vermis morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum posterior vermis morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum vermis lobule I morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis lobule I morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum vermis lobule IX morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis lobule IX morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum vermis lobule X morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis lobule X morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum vermis lobule VIII morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum vermis lobule VIII morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Cerebellar vermis medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar vermis medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar vermis hypoplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar vermis hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dysgenesis of the cerebellar vermis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dysgenesis of the cerebellar vermis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormal cerebellar vermis morphology Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal cerebellar vermis morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.
amyloidosis, familial; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; amyloidosis, familial; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple familial trichoepithelioma and familial cylindromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple familial trichoepithelioma and familial cylindromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis, familial; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hemiplegic migraine and benign familial infantile convulsions Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Renal hypodysplasia/aplasia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal hypodysplasia/aplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mullerian aplasia and hyperandrogenism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aplasia cutis congenita Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Radial aplasia-thrombocytopenia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Radial aplasia-thrombocytopenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic nerve aplasia, bilateral Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic nerve aplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital bilateral aplasia of vas deferens Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital bilateral aplasia of vas deferens from the curated CTD Gene-Disease Associations dataset.
Red-Cell Aplasia, Pure Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Red-Cell Aplasia, Pure from the curated CTD Gene-Disease Associations dataset.
Craniosynostosis radial aplasia syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Craniosynostosis radial aplasia syndrome from the curated CTD Gene-Disease Associations dataset.
Aplasia of Lacrimal and Salivary Glands Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aplasia of Lacrimal and Salivary Glands from the curated CTD Gene-Disease Associations dataset.
Mullerian Aplasia and Hyperandrogenism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mullerian Aplasia and Hyperandrogenism from the curated CTD Gene-Disease Associations dataset.
pure red-cell aplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pure red-cell aplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anemia; kidney diseases; red-cell aplasia, pure Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; kidney diseases; red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
red-cell aplasia, pure Gene Set From GAD Gene-Disease Associations genes associated with the disease red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aplasia Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term aplasia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
aplasia/hypoplasia involving the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the aplasia/hypoplasia involving the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
aplasia/hypoplasia of the cerebrum Gene Set From GWASdb SNP-Phenotype Associations genes associated with the aplasia/hypoplasia of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
aplasia/hypoplasia of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting the eye Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia cutis congenita of scalp Gene Set From HPO Gene-Disease Associations genes associated with the aplasia cutis congenita of scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the fallopian tube Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the uterus Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lacrimal gland aplasia Gene Set From HPO Gene-Disease Associations genes associated with the lacrimal gland aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the uvula Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the uvula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the tragus Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tragus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the nose Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the frontal sinuses Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the lungs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the lungs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the tarsal bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the quadriceps Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the quadriceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
biceps aplasia Gene Set From HPO Gene-Disease Associations genes associated with the biceps aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the musculature of the upper arm Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mandibular aplasia Gene Set From HPO Gene-Disease Associations genes associated with the mandibular aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the scapulae Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the scapulae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the abdominal wall musculature Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the skin Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of toe Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the iris Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the iris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the middle phalanx of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the middle phalanx of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lacrimal duct aplasia Gene Set From HPO Gene-Disease Associations genes associated with the lacrimal duct aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the pyramidal tract Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving forearm bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving forearm bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the sternum Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the sternum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the optic nerve Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the optic nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the ovary Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the corticospinal tracts Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the tarsal bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of metacarpal bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of metacarpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the ulna Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the feet Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia cutis congenita over posterior parietal area Gene Set From HPO Gene-Disease Associations genes associated with the aplasia cutis congenita over posterior parietal area phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the biceps Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the biceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting the fundus Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the fundus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting the retina Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the gallbladder Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the gallbladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the fingers Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the pelvis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the mandible Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the epiglottis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of metatarsal bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of metatarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the uterus Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
patellar aplasia Gene Set From HPO Gene-Disease Associations genes associated with the patellar aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the eyebrow Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the ovary Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the spleen Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the spleen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplastia of the eccrine sweat glands Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplastia of the eccrine sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the choroid Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the choroid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the semicircular canal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the semicircular canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mandibular condyle aplasia Gene Set From HPO Gene-Disease Associations genes associated with the mandibular condyle aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the lower limbs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the triceps Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the triceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
quadriceps aplasia Gene Set From HPO Gene-Disease Associations genes associated with the quadriceps aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the nose Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanges of the toes Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal hypoplasia/aplasia Gene Set From HPO Gene-Disease Associations genes associated with the renal hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia cutis congenita Gene Set From HPO Gene-Disease Associations genes associated with the aplasia cutis congenita phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting bones of the axial skeleton Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting bones of the axial skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bilateral radial aplasia Gene Set From HPO Gene-Disease Associations genes associated with the bilateral radial aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 1st metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the earlobes Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the earlobes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 4th metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 4th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of fingers Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the epiglottis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the radius Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the thymus Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 2nd metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 2nd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the skeleton Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the humerus Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the humerus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the palmar creases Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the maxilla Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the maxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the testes Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the testes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the ribs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 1st metatarsal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 1st metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the vertebral column Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the vertebral column phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the metacarpal bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the metacarpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the nipples Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nipples phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 5th metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 5th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the capital femoral epiphysis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the proximal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the proximal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the ear Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the diaphragm Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the thymus Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the premaxilla Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the premaxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the cerebrum Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 3rd toe Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
carpal bone aplasia Gene Set From HPO Gene-Disease Associations genes associated with the carpal bone aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the bladder Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting the uvea Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the uvea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the sweat glands Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the femur Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the musculature Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting the anterior segment of the eye Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the nasal bone Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the middle phalanges of the toes Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the testes Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the testes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the thorax Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the optic tract Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the sweat glands Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral pulmonary vessel aplasia Gene Set From HPO Gene-Disease Associations genes associated with the peripheral pulmonary vessel aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the nails Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the corpus callosum Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
midclavicular aplasia Gene Set From HPO Gene-Disease Associations genes associated with the midclavicular aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia cutis congenita over the scalp vertex Gene Set From HPO Gene-Disease Associations genes associated with the aplasia cutis congenita over the scalp vertex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the brainstem Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the pectoralis major muscle Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the pectoralis major muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the abdominal wall musculature Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the inner ear Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triceps aplasia Gene Set From HPO Gene-Disease Associations genes associated with the triceps aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the fovea Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the fovea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the cochlea Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the sinuses Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anterior segment of eye aplasia Gene Set From HPO Gene-Disease Associations genes associated with the anterior segment of eye aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the femoral head and neck Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the optic tract Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the extremities Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the vagina Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the nasal septum Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia cutis congenita on trunk or limbs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia cutis congenita on trunk or limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the clavicles Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the clavicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the sacrum Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the sacrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the skull Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the skull phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the musculature of the pelvis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the musculature of the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia involving bones of the lower limbs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia involving bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the parotid gland Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the parotid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the tibia Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tibia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the patella Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the patella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the skeletal musculature Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the skeletal musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting the eyelid Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the eyelid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the vagina Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the breasts Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the breasts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the musculature of the extremities Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the pubic bone Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia involving bones of the extremities Gene Set From HPO Gene-Disease Associations genes associated with the aplasia involving bones of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the pancreas Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the cervical spine Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cervical spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the cerebellum Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebellum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the carpal bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the toes Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia involving forearm bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia involving forearm bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
breast aplasia Gene Set From HPO Gene-Disease Associations genes associated with the breast aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the lens Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the lens phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the inner ear Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the external ear Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the external ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the shoulder musculature Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the shoulder musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the middle phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia cutis congenita over parietal area Gene Set From HPO Gene-Disease Associations genes associated with the aplasia cutis congenita over parietal area phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the vertebrae Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia involving bones of the upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the musculature of the upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the tongue Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tongue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the colon Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the colon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 3rd metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pectoral muscle hypoplasia/aplasia Gene Set From HPO Gene-Disease Associations genes associated with the pectoral muscle hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fibular aplasia Gene Set From HPO Gene-Disease Associations genes associated with the fibular aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the macula Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the macula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the musculature of the thigh Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the musculature of the thigh phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the middle phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the fibula Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal hypodysplasia/aplasia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the renal hypodysplasia/aplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
aplasia of lacrimal and salivary glands Gene Set From OMIM Gene-Disease Associations genes associated with the aplasia of lacrimal and salivary glands phenotype from the curated OMIM Gene-Disease Associations dataset.
patella aplasia or hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the patella aplasia or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
?renal hypodysplasia/aplasia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?renal hypodysplasia/aplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
mullerian aplasia and hyperandrogenism Gene Set From OMIM Gene-Disease Associations genes associated with the mullerian aplasia and hyperandrogenism phenotype from the curated OMIM Gene-Disease Associations dataset.
aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
?aplasia cutis congenita, nonsyndromic Gene Set From OMIM Gene-Disease Associations genes associated with the ?aplasia cutis congenita, nonsyndromic phenotype from the curated OMIM Gene-Disease Associations dataset.
?breasts and/or nipples, aplasia or hypoplasia of, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?breasts and/or nipples, aplasia or hypoplasia of, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Aplasia Of The Semicircular Canal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of The Semicircular Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia Cutis Congenita Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Cutis Congenita in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pure Red-Cell Aplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pure Red-Cell Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tibial Aplasia And Ectrodactyly Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tibial Aplasia And Ectrodactyly Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Bilateral Aplasia Of Vas Deferens Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Bilateral Aplasia Of Vas Deferens in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vas Deferens, Congenital Bilarteral, Aplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vas Deferens, Congenital Bilarteral, Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia/Hypoplasia Of The Thymus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The Thymus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Dysplasia And Retinal Aplasia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Dysplasia And Retinal Aplasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pectoral Muscle Hypoplasia/Aplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pectoral Muscle Hypoplasia/Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia Cutis Congenita Of Scalp Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Cutis Congenita Of Scalp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia Cutis Congenita Over Posterior Parietal Area Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Cutis Congenita Over Posterior Parietal Area in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia Of The Bone Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of The Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
B-Cell Aplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease B-Cell Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Nerve Aplasia, Bilateral Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Nerve Aplasia, Bilateral in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia/Hypoplasia Of The Iris Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The Iris in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia Cutis Congenita Over The Scalp Vertex Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Cutis Congenita Over The Scalp Vertex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia Of The Epiglottis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of The Epiglottis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia Of Muscle Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mullerian Aplasia And Hyperandrogenism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mullerian Aplasia And Hyperandrogenism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hydranencephaly With Renal Aplasia-Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hydranencephaly With Renal Aplasia-Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia/Hypoplasia Of The Earlobes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The Earlobes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Radial Aplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Radial Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia/Hypoplasia Of The Capital Femoral Epiphysis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The Capital Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Aplasia Of Inner Ear Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Aplasia Of Inner Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia/Hypoplasia Of The Extremities Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The Extremities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia/Hypoplastia Of The Eccrine Sweat Glands Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplastia Of The Eccrine Sweat Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thumb Aplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thumb Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia Of Lacrimal And Salivary Glands Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of Lacrimal And Salivary Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia Of The Parotid Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of The Parotid Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lacrimal Duct Aplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lacrimal Duct Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mullerian Aplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mullerian Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia Cutis Congenita With Epibulbar Dermoids Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Cutis Congenita With Epibulbar Dermoids in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia Of The Pectoralis Major Muscle Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of The Pectoralis Major Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Wilms Tumor And Radial Bilateral Aplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Wilms Tumor And Radial Bilateral Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Breasts And/Or Nipples, Aplasia Or Hypoplasia Of, 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Breasts And/Or Nipples, Aplasia Or Hypoplasia Of, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Patellar Aplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Patellar Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia/Hypoplasia Of The 5Th Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplasia/Hypoplasia Of The Abdominal Wall Musculature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Abdominal Wall Musculature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Eyebrow Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Eyebrow in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Bone Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Breasts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Breasts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Nails Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Nails in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Corpus Callosum Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Corpus Callosum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Cerebellum Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Cerebellum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Frontal Sinuses Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Frontal Sinuses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fibular Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibular Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Skin Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Renal Hypoplasia/Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Renal Hypoplasia/Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Fallopian Tube Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Fallopian Tube in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Cutis Congenita On Trunk Or Limbs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Cutis Congenita On Trunk Or Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Patellar Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Patellar Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Involving The Central Nervous System Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Involving The Skeletal Musculature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Skeletal Musculature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Tongue Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Uterus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Proximal Phalanges Of The Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Proximal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Involving The Metacarpal Bones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Metacarpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The 1St Metacarpal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The 1St Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of Fingers Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Uvula Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Uvula in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Nipples Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Nipples in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Lungs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Lungs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Abdominal Wall Musculature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Abdominal Wall Musculature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Sweat Glands Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Sweat Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Involving The Pelvis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Pelvis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of Optic Nerve Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of Optic Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The 3Rd Toe Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The 3Rd Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Affecting The Eye Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Affecting The Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The External Ear Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The External Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mandibular Condyle Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mandibular Condyle Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Ulna Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Ulna in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Lacrimal Gland Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lacrimal Gland Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Clavicles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Clavicles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anterior Segment Of Eye Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Segment Of Eye Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Bladder Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Bladder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Diaphragm Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Diaphragm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Gallbladder Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Gallbladder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pancreatic Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pancreatic Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of Metatarsal Bones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of Metatarsal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Involving The Nose Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Vagina Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Vagina in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Pancreas Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of Metacarpal Bones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of Metacarpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Phalanges Of The Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Tarsal Bones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Tarsal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Carpal Bone Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Carpal Bone Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Phalanges Of The 3Rd Toe Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Phalanges Of The 3Rd Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Biceps Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Biceps Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Quadriceps Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Quadriceps Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Triceps Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Triceps Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Lens Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Lens in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Vagina Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Vagina in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Midclavicular Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Midclavicular Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Optic Nerve Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Optic Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Bilateral Radial Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bilateral Radial Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Unilateral Radial Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unilateral Radial Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Pulmonary Vessel Aplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Pulmonary Vessel Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Involving The Carpal Bones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Testes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Testes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pure red-cell aplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Pure red-cell aplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Mullerian aplasia and hyperandrogenism Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Mullerian aplasia and hyperandrogenism from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Mullerian aplasia and hyperandrogenism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mullerian aplasia and hyperandrogenism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bilateral renal aplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bilateral renal aplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pure red-cell aplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pure red-cell aplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Aplasia of lacrimal and salivary glands Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aplasia of lacrimal and salivary glands in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Renal hypodysplasia/aplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal hypodysplasia/aplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Renal dysplasia and retinal aplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal dysplasia and retinal aplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital bilateral aplasia of vas deferens from CFTR mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital bilateral aplasia of vas deferens from CFTR mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Radial aplasia-thrombocytopenia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Radial aplasia-thrombocytopenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant aplasia and myelodysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant aplasia and myelodysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aplasia/Hypoplasia of the phalanges of the hand Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aplasia/Hypoplasia of the phalanges of the hand phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aplasia/Hypoplasia involving the metacarpal bones Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aplasia/Hypoplasia involving the metacarpal bones phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aplasia/Hypoplasia of the corpus callosum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aplasia/Hypoplasia of the corpus callosum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mullerian aplasia and hyperandrogenism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aplasia/Hypoplasia of the cerebellum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aplasia/Hypoplasia of the cerebellum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial Mediterranean fever Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial Mediterranean fever phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytosis, benign familial microcytic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytosis, benign familial microcytic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal-infantile seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neurofibromatosis, familial spinal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neurofibromatosis, familial spinal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tumoral calcinosis, familial, hyperphosphatemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, hyperphosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial restrictive cardiomyopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial restrictive cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaze palsy, familial horizontal, with progressive scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hemiplegic migraine type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hemiplegic migraine type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythrocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial neonatal seizures 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial neonatal seizures 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperuricemic nephropathy, familial juvenile, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemic nephropathy, familial juvenile, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cancer of breast Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cancer of breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign pemphigus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign pemphigus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperpigmentation, familial progressive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial aortopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial aortopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Digital arthropathy-brachydactyly, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Digital arthropathy-brachydactyly, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial benign hypercalcemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial benign hypercalcemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial visceral amyloidosis, Ostertag type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial visceral amyloidosis, Ostertag type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dementia familial British Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dementia familial British phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial porencephaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial porencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
familial hyperinsulinism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the familial hyperinsulinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperinsulinemic hypoglycemia familial 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinemic hypoglycemia familial 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Febrile seizures, familial, 3b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Febrile seizures, familial, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Paroxysmal familial ventricular fibrillation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypercholesterolemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypercholesterolemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hidradenitis suppurativa, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hidradenitis suppurativa, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dementia, familial Danish Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dementia, familial Danish phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign familial hematuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign familial hematuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial dysautonomia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial dysautonomia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial febrile seizures 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial febrile seizures 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fleck retina, familial benign Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fleck retina, familial benign phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked familial exudative vitreoretinopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked familial exudative vitreoretinopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial colorectal cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial colorectal cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial porphyria cutanea tarda Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial porphyria cutanea tarda phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced sleep phase syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonus, familial cortical Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonus, familial cortical phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Migraine, familial basilar Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Migraine, familial basilar phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Breast-ovarian cancer, familial 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Breast-ovarian cancer, familial 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercholanemia, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercholanemia, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone marrow failure, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bone marrow failure, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced sleep phase syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Candidiasis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Candidiasis, familial, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypokalemia-hypomagnesemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypokalemia-hypomagnesemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenia, limb-girdle, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenia, limb-girdle, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemophagocytic lymphohistiocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular fibrillation, paroxysmal familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular fibrillation, paroxysmal familial, 2 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.
Familial erythrocytosis, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial erythrocytosis, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial medullary thyroid carcinoma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperlipidemia, familial combined Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperlipidemia, familial combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial amyloid polyneuropathy, Iowa type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial amyloid polyneuropathy, Iowa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial encephalopathy with neuroserpin inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, familial adult myoclonic, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, familial adult myoclonic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial myxoma, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial myxoma, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, familial partial, type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, familial partial, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, familial partial, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, familial partial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalciuric hypercalcemia, familial, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalciuric hypercalcemia, familial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial multiple polyposis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial juvenile gout Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial juvenile gout phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypobetalipoproteinemia, familial, associated with apob32 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypobetalipoproteinemia, familial, associated with apob32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Breast-ovarian cancer, familial 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Breast-ovarian cancer, familial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial fibrillation, familial, 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial fibrillation, familial, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary familial hypertrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary familial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial type 3 hyperlipoproteinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial type 3 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tumoral calcinosis, familial, normophosphatemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tumoral calcinosis, familial, normophosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cd8 deficiency, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial infantile myasthenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked familial atypical mycobacteriosis, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked familial atypical mycobacteriosis, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperthyroxinemia, familial dysalbuminemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperthyroxinemia, familial dysalbuminemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial type 5 hyperlipoproteinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial type 5 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutaneous telangiectasia and cancer syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial renal glucosuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial renal glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial pulmonary capillary hemangiomatosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypoalphalipoproteinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypoalphalipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial renal hypouricemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial renal hypouricemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
HYPERALDOSTERONISM, FAMILIAL, TYPE III Gene Set From ClinVar Gene-Phenotype Associations genes associated with the HYPERALDOSTERONISM, FAMILIAL, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonic epilepsy, familial infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypoplastic, glomerulocystic kidney Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypoplastic, glomerulocystic kidney phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cold urticaria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cold urticaria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic Aneurysm, Familial Abdominal 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 2 from the curated CTD Gene-Disease Associations dataset.
Familial myelofibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial myelofibrosis from the curated CTD Gene-Disease Associations dataset.
Nephronophthisis, familial juvenile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephronophthisis, familial juvenile from the curated CTD Gene-Disease Associations dataset.
Eosinophilia, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Eosinophilia, Familial from the curated CTD Gene-Disease Associations dataset.
Hyperlipidemia, Familial Combined Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperlipidemia, Familial Combined 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.
Hyperinsulinemic hypoglycemia, familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 6 from the curated CTD Gene-Disease Associations dataset.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.
Pemphigus, Benign Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pemphigus, Benign Familial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 1 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 9 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 8 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 6 from the curated CTD Gene-Disease Associations dataset.
Amyloidosis, familial visceral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, familial visceral from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Hypertrophic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Hypertrophic, Familial from the curated CTD Gene-Disease Associations dataset.
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaze Palsy, Familial Horizontal, with Progressive Scoliosis from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 8 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 7 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 1 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 2 from the curated CTD Gene-Disease Associations dataset.
Myasthenia, Familial Infantile, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myasthenia, Familial Infantile, 1 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Abdominal 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 1 from the curated CTD Gene-Disease Associations dataset.
STUTTERING, FAMILIAL PERSISTENT, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease STUTTERING, FAMILIAL PERSISTENT, 1 from the curated CTD Gene-Disease Associations dataset.
Dementia, familial British Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dementia, familial British from the curated CTD Gene-Disease Associations dataset.
Candidiasis familial chronic mucocutaneous, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis familial chronic mucocutaneous, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Gliosis, Familial Progressive Subcortical Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gliosis, Familial Progressive Subcortical from the curated CTD Gene-Disease Associations dataset.
CD8 Deficiency, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CD8 Deficiency, Familial from the curated CTD Gene-Disease Associations dataset.
Insomnia, Fatal Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Insomnia, Fatal Familial from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset.
Familial HDL deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial HDL deficiency from the curated CTD Gene-Disease Associations dataset.
Familial dermographism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial dermographism from the curated CTD Gene-Disease Associations dataset.
Candidiasis, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis, Familial, 3 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.
Erythrocytosis, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Erythrocytosis, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Visceral Myopathy, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Visceral Myopathy, Familial from the curated CTD Gene-Disease Associations dataset.
Hyperthyroidism, Familial Gestational Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperthyroidism, Familial Gestational from the curated CTD Gene-Disease Associations dataset.
Hematuria, Benign Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hematuria, Benign Familial from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL INFANTILE, 2 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Migraine, Familial Hemiplegic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Migraine, Familial Hemiplegic, 3 from the curated CTD Gene-Disease Associations dataset.
FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.
Cancer, Familial, with In Vitro Radioresistance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cancer, Familial, with In Vitro Radioresistance from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Hypoparathyroidism familial isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypoparathyroidism familial isolated from the curated CTD Gene-Disease Associations dataset.
Tumoral Calcinosis, Hyperphosphatemic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tumoral Calcinosis, Hyperphosphatemic, Familial from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Hidradenitis suppurativa, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hidradenitis suppurativa, familial from the curated CTD Gene-Disease Associations dataset.
Dementia, familial Danish Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dementia, familial Danish from the curated CTD Gene-Disease Associations dataset.
Familial medullary thyroid carcinoma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial medullary thyroid carcinoma from the curated CTD Gene-Disease Associations dataset.
Interstitial Pneumonitis, Desquamative, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Interstitial Pneumonitis, Desquamative, Familial from the curated CTD Gene-Disease Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 4 from the curated CTD Gene-Disease Associations dataset.
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset.
Cirrhosis, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cirrhosis, Familial from the curated CTD Gene-Disease Associations dataset.
Familial encephalopathy with neuroserpin inclusion bodies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Familial Partial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Familial Partial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 3 from the curated CTD Gene-Disease Associations dataset.
Familial Mediterranean Fever, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Familial Hypophosphatemic Rickets Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Hypophosphatemic Rickets from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.
Keratoacanthoma familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Keratoacanthoma familial from the curated CTD Gene-Disease Associations dataset.
Hepatic Adenomas, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Adenomas, Familial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 10 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 13 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 15 from the curated CTD Gene-Disease Associations dataset.
Familial Wilms tumor 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Wilms tumor 2 from the curated CTD Gene-Disease Associations dataset.
Candidiasis, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 9 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic Hypoglycemia, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic Hypoglycemia, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Familial antiphospholipid syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial antiphospholipid syndrome from the curated CTD Gene-Disease Associations dataset.
Amyloidosis, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, Familial from the curated CTD Gene-Disease Associations dataset.
Familial paroxysmal dystonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial paroxysmal dystonia from the curated CTD Gene-Disease Associations dataset.
Atrial fibrillation, familial 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial fibrillation, familial 1 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Hypercholanemia, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypercholanemia, Familial from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Hyperbilirubinemia, Transient Familial Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperbilirubinemia, Transient Familial Neonatal from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 from the curated CTD Gene-Disease Associations dataset.
Meningioma, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Meningioma, familial from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 6 from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 2 from the curated CTD Gene-Disease Associations dataset.
Dysautonomia, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dysautonomia, Familial from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 1 from the curated CTD Gene-Disease Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 3 from the curated CTD Gene-Disease Associations dataset.
Familial Cold Autoinflammatory Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Cold Autoinflammatory Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Familial Adult Myoclonic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Adult Myoclonic, 3 from the curated CTD Gene-Disease Associations dataset.
Prostate cancer, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prostate cancer, familial from the curated CTD Gene-Disease Associations dataset.
Convulsions, Benign Familial Infantile, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset.
Polycythemia, primary familial and congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset.
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 1 from the curated CTD Gene-Disease Associations dataset.
Erythrocytosis, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocytosis, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 3 from the curated CTD Gene-Disease Associations dataset.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.
Hyperinsulinemic hypoglycemia, familial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 7 from the curated CTD Gene-Disease Associations dataset.
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset.
Hyperthyroxinemia, Familial Dysalbuminemic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperthyroxinemia, Familial Dysalbuminemic from the curated CTD Gene-Disease Associations dataset.
Aortic aneurysm, familial thoracic 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic aneurysm, familial thoracic 4 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 2 from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Familial cylindromatosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial cylindromatosis from the curated CTD Gene-Disease Associations dataset.
Familial benign hypercalcemia, type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial benign hypercalcemia, type 3 from the curated CTD Gene-Disease Associations dataset.
Hyperaldosteronism, Familial, Type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperaldosteronism, Familial, Type II from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 11 from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.
Atrial myxoma, familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial myxoma, familial from the curated CTD Gene-Disease Associations dataset.
Familial Glucocorticoid Deficiency 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Glucocorticoid Deficiency 1 from the curated CTD Gene-Disease Associations dataset.
Tumoral Calcinosis, Normophosphatemic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tumoral Calcinosis, Normophosphatemic, Familial from the curated CTD Gene-Disease Associations dataset.
MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.
Hypocalciuric hypercalcemia, familial, type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypocalciuric hypercalcemia, familial, type 1 from the curated CTD Gene-Disease Associations dataset.
Trichoepithelioma multiple familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma multiple familial from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 10 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 from the curated CTD Gene-Disease Associations dataset.
Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 2 from the curated CTD Gene-Disease Associations dataset.
Periodic fever, familial, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Periodic fever, familial, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
VENTRICULAR TACHYCARDIA, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset.
Hyperuricemic Nephropathy, Familial Juvenile 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperuricemic Nephropathy, Familial Juvenile 2 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, Apolipoprotein B from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Abdominal 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 3 from the curated CTD Gene-Disease Associations dataset.
Familial schizencephaly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial schizencephaly from the curated CTD Gene-Disease Associations dataset.
Atrial Fibrillation, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Fibrillation, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 from the curated CTD Gene-Disease Associations dataset.
Neurofibromatosis, Familial Spinal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neurofibromatosis, Familial Spinal from the curated CTD Gene-Disease Associations dataset.
Reticuloendotheliosis, familial, with eosinophilia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Reticuloendotheliosis, familial, with eosinophilia from the curated CTD Gene-Disease Associations dataset.
SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 from the curated CTD Gene-Disease Associations dataset.
Advanced Sleep-Phase Syndrome, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Advanced Sleep-Phase Syndrome, Familial from the curated CTD Gene-Disease Associations dataset.
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 2 from the curated CTD Gene-Disease Associations dataset.
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 1 from the curated CTD Gene-Disease Associations dataset.
MITRAL VALVE PROLAPSE, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MITRAL VALVE PROLAPSE, FAMILIAL from the curated CTD Gene-Disease Associations dataset.
Progressive Familial Heart Block, Type Ib Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive Familial Heart Block, Type Ib from the curated CTD Gene-Disease Associations dataset.
Familial dilated cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial dilated cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 3 from the curated CTD Gene-Disease Associations dataset.
Thymoma, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thymoma, Familial from the curated CTD Gene-Disease Associations dataset.
Atypical Mycobacteriosis, Familial, X-Linked 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.
Familial Testotoxicosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Testotoxicosis from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Myoclonic, Benign Adult Familial, Type 1 from the curated CTD Gene-Disease Associations dataset.
Hemiplegic migraine, familial type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemiplegic migraine, familial type 2 from the curated CTD Gene-Disease Associations dataset.
Hemiplegic migraine, familial type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hemiplegic migraine, familial type 1 from the curated CTD Gene-Disease Associations dataset.
Familial apoceruloplasmin deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial apoceruloplasmin deficiency from the curated CTD Gene-Disease Associations dataset.
HYPERCHOLESTEROLEMIA, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERCHOLESTEROLEMIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset.
Amyloid Neuropathies, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Amyloid Neuropathies, Familial from the curated CTD Gene-Disease Associations dataset.
CANDIDIASIS, FAMILIAL, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CANDIDIASIS, FAMILIAL, 2 from the curated CTD Gene-Disease Associations dataset.
Familial Mediterranean Fever Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Mediterranean Fever from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 7 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Febrile Convulsions, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Febrile Convulsions, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Cerebral Amyloid Angiopathy, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral Amyloid Angiopathy, Familial from the curated CTD Gene-Disease Associations dataset.
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 from the curated CTD Gene-Disease Associations dataset.
Hypobetalipoproteinemia, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Stuttering, Familial Persistent 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stuttering, Familial Persistent 2 from the curated CTD Gene-Disease Associations dataset.
Trichoepithelioma, Multiple Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trichoepithelioma, Multiple Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Familial Temporal Lobe, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Familial Temporal Lobe, 4 from the curated CTD Gene-Disease Associations dataset.
MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 14 from the curated CTD Gene-Disease Associations dataset.
familial mediterranean fever Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial mediterranean fever from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial adenomatous polyposis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial adenomatous polyposis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial hyperlipidemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial hyperlipidemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial hemiplegic migraine Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial hemiplegic migraine from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial atrial fibrillation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial atrial fibrillation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial juvenile hyperuricemic nephropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial juvenile hyperuricemic nephropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial lipoprotein lipase deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial periodic paralysis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial periodic paralysis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
familial lipoprotein lipase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hypertriglyceridemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hypertriglyceridemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial infantile epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial adenomatous polyposis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial adenomatous polyposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial combined hyperlipidemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial combined hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial renal oncocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial renal oncocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fatal familial insomnia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fatal familial insomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial mediterranean fever Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial mediterranean fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial nephrotic syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial nephrotic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial glomangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial glomangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hyperlipidemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hypercholesterolemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hypercholesterolemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial periodic paralysis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial periodic paralysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial juvenile hyperuricemic nephropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial juvenile hyperuricemic nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
benign familial neonatal epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial partial lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial partial lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial hemiplegic migraine Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial hemiplegic migraine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial visceral amyloidosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial visceral amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial atrial fibrillation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial atrial fibrillation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial medullary thyroid carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial medullary thyroid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial renal papillary carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial renal papillary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial retinoblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial retinoblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial adenomatous polyposis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial adenomatous polyposis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; spondylitis, ankylosing Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial atypical progressive supranuclear palsy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial atypical progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial or sporadic prostate cancer. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial or sporadic prostate cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial distal renal tubular acidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever Gene Set From GAD Gene-Disease Associations genes associated with the disease abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial defective apolipoprotein b100. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b100. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypercholesterolaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid neuropathies; amyloid neuropathies, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies; amyloid neuropathies, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
early-onset familial alzheimer's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease early-onset familial alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abdomen, acute; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease abdomen, acute; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial dysbetalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial dysbetalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial defective apolipoprotein b Gene Set From GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloid polyneuropathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinson's disease (familial) Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinson's disease (familial) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild familial hypercholesterolaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial combined hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial combined hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endogenous hypertriglyceridemia and familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease endogenous hypertriglyceridemia and familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene Set From GAD Gene-Disease Associations genes associated with the disease familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial age-related macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease familial age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial premature myocardial infarction. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial premature myocardial infarction. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
late onset of familial adenomatous polyposis Gene Set From GAD Gene-Disease Associations genes associated with the disease late onset of familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloidotic polyneuropathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloidotic polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid neuropathies, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial defective apolipoprotein b-100 in a chinese man Gene Set From GAD Gene-Disease Associations genes associated with the disease familial defective apolipoprotein b-100 in a chinese man in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; familial mediterranean fever; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
premature coronary artery disease and familial hypoalphalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease premature coronary artery disease and familial hypoalphalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; familial mediterranean fever; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; familial mediterranean fever; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial male-limited precocious puberty. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial male-limited precocious puberty. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial combined hyperlipidaemia. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial combined hyperlipidaemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; familial mediterranean fever; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial early onset psoriasis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial early onset psoriasis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypobetalipoproteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypobetalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyotrophic lateral sclerosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyotrophic lateral sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloid polyneuropathy in a hungarian family. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy in a hungarian family. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial melanoma Gene Set From GAD Gene-Disease Associations genes associated with the disease familial melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
rapidly progressive familial amyotrophic lateral sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease rapidly progressive familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyotrophic lateral sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypocalciuric hypercalcemia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypocalciuric hypercalcemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial adenomatous polyposis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hyperinsulinism. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hyperinsulinism. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial glucocorticoid deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease familial glucocorticoid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
late onset familial adenomatous polyposis Gene Set From GAD Gene-Disease Associations genes associated with the disease late onset familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloid polyneuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloid polyneuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypercholesterolemia. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypercholesterolemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial partial lipodystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial partial lipodystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial amyloidotic polyneuropathy type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease familial amyloidotic polyneuropathy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; infertility, male Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial liver adenomatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial liver adenomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diarrhea; familial mediterranean fever; pain; stomatitis, aphthous Gene Set From GAD Gene-Disease Associations genes associated with the disease diarrhea; familial mediterranean fever; pain; stomatitis, aphthous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast cancer, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease breast cancer, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypertrophic cardiomyopathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypertrophic cardiomyopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease familial cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; arthritis, rheumatoid; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; arthritis, rheumatoid; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
creutzfeldt-jakob disease; creutzfeldt-jakob syndrome; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; creutzfeldt-jakob syndrome; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood pressure; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease blood pressure; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; atherosclerosis; familial mediterranean fever; Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; atherosclerosis; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene Set From GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial exudative vitreoretinopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial exudative vitreoretinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; arthritis, rheumatoid; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; arthritis, rheumatoid; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial dysautonomia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial dysautonomia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial alzheimer's disease associated Gene Set From GAD Gene-Disease Associations genes associated with the disease familial alzheimer's disease associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
greenland familial cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease greenland familial cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial diabetes insipidus Gene Set From GAD Gene-Disease Associations genes associated with the disease familial diabetes insipidus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial erythrocytosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial erythrocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial bronchiectasis. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial bronchiectasis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial non-ret c cell hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease familial non-ret c cell hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypertension of early onset. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypertension of early onset. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; hyperlipidemia, familial combined Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; hyper-igd syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; hyper-igd syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; fever Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term familial in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Familial combined hyperlipidaemia_Blood monocyte_GSE11393 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial combined hyperlipidaemia_Blood monocyte_GSE11393 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Familial combined hyperlipidaemia_lymphoblast_GSE1010 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial combined hyperlipidaemia_lymphoblast_GSE1010 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Familial hypophosphataemic rickets_Renal Tissue_GSE868 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Familial hypophosphataemic rickets_Renal Tissue_GSE868 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Parkinson's disease (familial) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Parkinson's disease (familial) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
familial hypertriglyceridemia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease familial hypertriglyceridemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
familial atrial fibrillation Gene Set From GWASdb SNP-Disease Associations genes associated with the disease familial atrial fibrillation in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
familial predisposition Gene Set From HPO Gene-Disease Associations genes associated with the familial predisposition phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hyperlipidemia, Familial Combined Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperlipidemia, Familial Combined phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Paralyses, Familial Periodic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Paralyses, Familial Periodic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cardiomyopathy, Hypertrophic, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cardiomyopathy, Hypertrophic, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Familial Mediterranean Fever Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Familial Mediterranean Fever phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Lipodystrophy, Familial Partial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lipodystrophy, Familial Partial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Amyloidosis, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Amyloidosis, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Dysautonomia, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dysautonomia, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Amyloid Neuropathies, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Amyloid Neuropathies, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Insomnia, Fatal Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Insomnia, Fatal Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, familial focal, with variable foci Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial focal, with variable foci phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperparathyroidism, familial primary Gene Set From OMIM Gene-Disease Associations genes associated with the hyperparathyroidism, familial primary phenotype from the curated OMIM Gene-Disease Associations dataset.
{atrial fibrillation, familial, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {atrial fibrillation, familial, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{breast-ovarian cancer, familial, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
digital arthropathy-brachydactyly, familial Gene Set From OMIM Gene-Disease Associations genes associated with the digital arthropathy-brachydactyly, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive familial heart block, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the progressive familial heart block, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial basilar Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial basilar phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 4 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 7 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 8 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 9 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
insomnia, fatal familial Gene Set From OMIM Gene-Disease Associations genes associated with the insomnia, fatal familial phenotype from the curated OMIM Gene-Disease Associations dataset.
dysautonomia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the dysautonomia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined hyperlipidemia, familial Gene Set From OMIM Gene-Disease Associations genes associated with the combined hyperlipidemia, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial abdominal 1 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial abdominal 2 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
familial cold-induced inflammatory syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the familial cold-induced inflammatory syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, familial temporal lobe, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, familial temporal lobe, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 19 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 18 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 15 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 16 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypobetalipoproteinemia, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hypobetalipoproteinemia, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 3a Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 3a phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic 17 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
dementia, familial danish Gene Set From OMIM Gene-Disease Associations genes associated with the dementia, familial danish phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
seizures, benign familial infantile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the seizures, benign familial infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
[igg receptor i, phagocytic, familial deficiency of] Gene Set From OMIM Gene-Disease Associations genes associated with the [igg receptor i, phagocytic, familial deficiency of] phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperuricemic nephropathy, familial juvenile 1 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{breast-ovarian cancer, familial, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {breast-ovarian cancer, familial, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperaldosteronism, familial, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the hyperaldosteronism, familial, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperinsulinemic hypoglycemia, familial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperinsulinemic hypoglycemia, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
?epilepsy, familial adult myoclonic, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the ?epilepsy, familial adult myoclonic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
?candidiasis, familial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the ?candidiasis, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
[fleck retina, familial benign] Gene Set From OMIM Gene-Disease Associations genes associated with the [fleck retina, familial benign] phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 21 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 22 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 22 phenotype from the curated OMIM Gene-Disease Associations dataset.
candidiasis, familial, 6, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the candidiasis, familial, 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
carpal tunnel syndrome, familial Gene Set From OMIM Gene-Disease Associations genes associated with the carpal tunnel syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 17 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 16 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial fibrillation, familial, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial fibrillation, familial, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
medullary thyroid carcinoma, familial Gene Set From OMIM Gene-Disease Associations genes associated with the medullary thyroid carcinoma, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercholesterolemia, familial, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the hypercholesterolemia, familial, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular fibrillation, paroxysmal familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
acne inversa, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the acne inversa, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
endometrial cancer, familial Gene Set From OMIM Gene-Disease Associations genes associated with the endometrial cancer, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperbilirubinemia, familial transient neonatal Gene Set From OMIM Gene-Disease Associations genes associated with the hyperbilirubinemia, familial transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.
dementia, familial, nonspecific Gene Set From OMIM Gene-Disease Associations genes associated with the dementia, familial, nonspecific phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperuricemic nephropathy, familial juvenile 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperuricemic nephropathy, familial juvenile, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperaldosteronism, familial, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the hyperaldosteronism, familial, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, familial partial, type 4 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, familial partial, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, familial partial, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, familial partial, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
amyloidosis, familial visceral Gene Set From OMIM Gene-Disease Associations genes associated with the amyloidosis, familial visceral phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
hematuria, familial benign Gene Set From OMIM Gene-Disease Associations genes associated with the hematuria, familial benign phenotype from the curated OMIM Gene-Disease Associations dataset.
hematuria, benign familial Gene Set From OMIM Gene-Disease Associations genes associated with the hematuria, benign familial phenotype from the curated OMIM Gene-Disease Associations dataset.
dementia, familial british Gene Set From OMIM Gene-Disease Associations genes associated with the dementia, familial british phenotype from the curated OMIM Gene-Disease Associations dataset.
pseudohyperkalemia, familial, 2, due to red cell leak Gene Set From OMIM Gene-Disease Associations genes associated with the pseudohyperkalemia, familial, 2, due to red cell leak phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenia, limb-girdle, familial Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenia, limb-girdle, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
[erythrocytosis, familial, 1] Gene Set From OMIM Gene-Disease Associations genes associated with the [erythrocytosis, familial, 1] phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, familial, with neuroserpin inclusion bodies Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, familial, with neuroserpin inclusion bodies phenotype from the curated OMIM Gene-Disease Associations dataset.
{migraine, familial typical, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {migraine, familial typical, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperpigmentation, familial progressive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperpigmentation, familial progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 4 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.
thrombophilia, familial, due to decreased release of plat Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia, familial, due to decreased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.
cylindromatosis, familial Gene Set From OMIM Gene-Disease Associations genes associated with the cylindromatosis, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
dyskinesia, familial, with facial myokymia Gene Set From OMIM Gene-Disease Associations genes associated with the dyskinesia, familial, with facial myokymia phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic pain syndrome, familial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
episodic pain syndrome, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the episodic pain syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypoparathyroidism, familial isolated Gene Set From OMIM Gene-Disease Associations genes associated with the hypoparathyroidism, familial isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
gastrointestinal stromal tumor, familial Gene Set From OMIM Gene-Disease Associations genes associated with the gastrointestinal stromal tumor, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
{aneurysm, familial abdominal 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {aneurysm, familial abdominal 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
hemophagocytic lymphohistiocytosis, familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hemophagocytic lymphohistiocytosis, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
febrile seizures, familial, 3b Gene Set From OMIM Gene-Disease Associations genes associated with the febrile seizures, familial, 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
advanced sleep phase syndrome, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the advanced sleep phase syndrome, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
stuttering, familial persistent, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the stuttering, familial persistent, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
stuttering, familial persistent, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the stuttering, familial persistent, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

Harmonizome 3.0

PTLAH Gene

AAA1 Gene

AAA3 Gene

AAA2 Gene

AAA4 Gene

ETL6 Gene

RCM2 Gene

ATFB8 Gene

HNFJ3 Gene

GPSC Gene

BHD Gene

FAME4 Gene

FAME3 Gene

PFHB2 Gene

BFIS1 Gene

HBN1 Gene

ETL2 Gene

FHII Gene

FCMTE2 Gene

FCMTE1 Gene

GLM4 Gene

PSHK2 Gene

VVS Gene

BFIS4 Gene

ATFB1 Gene

ATFB2 Gene

SXI2 Gene

BFIC2 Gene

FMTLE Gene

STUT3 Gene

STUT2 Gene

STUT1 Gene

STUT4 Gene

BRCD1 Gene

MGR2 Gene

MGR3 Gene

MFT2 Gene

FEB9 Gene

ATFB5 Gene

HTGS Gene

DIP Gene

CMH21 Gene

CANDF1 Gene

ATPLS Gene

EOS Gene

FEB10 Gene

LVNC2 Gene

THCYTX Gene

CMS1A1 Gene

BPPV Gene

AAT2 Gene

AAT1 Gene

NKCD Gene

Familial Aplasia Of The Vermis Gene Set

aplasia of the inferior half of the cerebellar vermis Gene Set

aplasia/hypoplasia of the cerebellar vermis Gene Set

Aplasia/Hypoplasia Of The Cerebellar Vermis Gene Set

Aplasia Of The Inferior Half Of The Cerebellar Vermis Gene Set

mantle zone of cerebellar vermis Gene Set

white matter of cerebellar vermis Gene Set

cerebellar vermis Gene Set

cortex of cerebellar vermis Gene Set

superficial stratum of cerebellar vermis Gene Set

Folium-tuber vermis (VII), granular layer Gene Set

Folium-tuber vermis (VII), molecular layer Gene Set

Folium-tuber vermis (VII) Gene Set

intermediate stratum of cerebellar vermis Gene Set

periventricular stratum of cerebellar vermis Gene Set

cerebellar vermis Gene Set

vermis Gene Set

agenesis of cerebellar vermis Gene Set

dysgenesis of the cerebellar vermis Gene Set

cerebellar vermis atrophy Gene Set

inferior vermis hypoplasia Gene Set

cerebellar vermis hypoplasia Gene Set

disorganization of the anterior cerebellar vermis Gene Set

abnormality of the cerebellar vermis Gene Set

loss of purkinje cells in the cerebellar vermis Gene Set

abnormal cerebellum posterior vermis morphology Gene Set