Results for "Neurodevelopmental delay": 258 gene sets

Name

neurodevelopmental delay Gene Set

From HPO Gene-Disease Associations

genes associated with the neurodevelopmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Neurodevelopmental Delay Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Neurodevelopmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Neurodevelopmental delay Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Neurodevelopmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Severe neurodevelopmental delay Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Severe neurodevelopmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Growth retardation, developmental delay, coarse facies, and early death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, hyperphagia, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset.

Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.

Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset.

delay discounting Gene Set

From GAD Gene-Disease Associations

genes associated with the disease delay discounting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

delay Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term delay in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

moderate global developmental delay Gene Set

From HPO Gene-Disease Associations

genes associated with the moderate global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

motor delay Gene Set

From HPO Gene-Disease Associations

genes associated with the motor delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe carpal ossification delay Gene Set

From HPO Gene-Disease Associations

genes associated with the severe carpal ossification delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mild global developmental delay Gene Set

From HPO Gene-Disease Associations

genes associated with the mild global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

marked delay in bone age Gene Set

From HPO Gene-Disease Associations

genes associated with the marked delay in bone age phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

global developmental delay Gene Set

From HPO Gene-Disease Associations

genes associated with the global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

growth delay Gene Set

From HPO Gene-Disease Associations

genes associated with the growth delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

expressive language delay Gene Set

From HPO Gene-Disease Associations

genes associated with the expressive language delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe global developmental delay Gene Set

From HPO Gene-Disease Associations

genes associated with the severe global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

obesity, hyperphagia, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, hyperphagia, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, seizures, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, seizures, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

?obesity, hyperphagia, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?obesity, hyperphagia, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

growth retardation, developmental delay, coarse facies, and early death Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth retardation, developmental delay, coarse facies, and early death phenotype from the curated OMIM Gene-Disease Associations dataset.

sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

Global Developmental Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Clumsiness - Motor Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Clumsiness - Motor Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Developmental Delay, Epilepsy, And Neonatal Diabetes Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Developmental Delay, Epilepsy, And Neonatal Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Mild Expressive Language Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Mild Expressive Language Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Speech Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Speech Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Gross Motor Development Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Gross Motor Development Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Profound Global Developmental Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Profound Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Severe Expressive Language Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Severe Expressive Language Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Brachycephaly, Trichomegaly, And Developmental Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Brachycephaly, Trichomegaly, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Receptive Language Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Receptive Language Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Constitutional Delay Of Puberty Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Constitutional Delay Of Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Constitutional Delay Of Growth And Puberty Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Constitutional Delay Of Growth And Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Developmental Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Moderate Expressive Language Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Moderate Expressive Language Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Severe Receptive Language Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Severe Receptive Language Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Developmental And Speech Delay Due To Sox5 Deficiency Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Developmental And Speech Delay Due To Sox5 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Plantar Lipomatosis, Unusual Facies, And Developmental Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Plantar Lipomatosis, Unusual Facies, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Thoc6-Related Developmental Delay-Microcephaly-Facial Dysmorphism Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Thoc6-Related Developmental Delay-Microcephaly-Facial Dysmorphism Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cardiac, Facial, And Digital Anomalies With Developmental Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cardiac, Facial, And Digital Anomalies With Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Developmental Delay (Disorder) Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Developmental Delay (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Severe Global Developmental Delay Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Severe Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Growth Delay Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Growth Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Mild Global Developmental Delay Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Mild Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Motor Delay Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Motor Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Moderate Global Developmental Delay Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Moderate Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Expressive Language Delay Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Expressive Language Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Language Delay Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Language Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Severe Speech Delay Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Severe Speech Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Marked Delay In Bone Age Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Marked Delay In Bone Age in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Severe Achondrodysplasia With Developmental Delay And Acanthosis Nigricans Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Severe Achondrodysplasia With Developmental Delay And Acanthosis Nigricans in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Pili Torti Developmental Delay Neurological Abnormalities Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Pili Torti Developmental Delay Neurological Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Developmental Delay, Mild Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Developmental Delay, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Moderate Receptive Language Delay Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Moderate Receptive Language Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Severe Carpal Ossification Delay Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Severe Carpal Ossification Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

behavioral developmental delay Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the behavioral developmental delay phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

motor developmental delay Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the motor developmental delay phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

microcephaly, seizures, and developmental delay Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease microcephaly, seizures, and developmental delay from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

microcephaly, seizures, and developmental delay Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease microcephaly, seizures, and developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intellectual disability-severe speech delay-mild dysmorphism syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intellectual disability-severe speech delay-mild dysmorphism syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Developmental delay and seizures with or without movement abnormalities Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Developmental delay and seizures with or without movement abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Congenital limbs-face contractures-hypotonia-developmental delay syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Congenital limbs-face contractures-hypotonia-developmental delay syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

brachycephaly, trichomegaly, and developmental delay Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease brachycephaly, trichomegaly, and developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Developmental delay, hypotonia, and impaired language Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Developmental delay, hypotonia, and impaired language in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Global developmental delay Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Global developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cardiac anomalies - developmental delay - facial dysmorphism syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cardiac anomalies - developmental delay - facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Severe global developmental delay Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Severe global developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Growth delay due to insulin-like growth factor I resistance Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Growth delay due to insulin-like growth factor I resistance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Severe achondroplasia-developmental delay-acanthosis nigricans syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Severe achondroplasia-developmental delay-acanthosis nigricans syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Intellectual disability-severe speech delay-mild dysmorphism syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Intellectual disability-severe speech delay-mild dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Developmental delay and seizures Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Developmental delay and seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Developmental delay Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Macrocephaly-developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Macrocephaly-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Pancytopenia-developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Pancytopenia-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Growth delay Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Growth delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Moderate global developmental delay Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Moderate global developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

GNAO1-related developmental delay-seizures-movement disorder spectrum Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the GNAO1-related developmental delay-seizures-movement disorder spectrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Spastic paraplegia-severe developmental delay-epilepsy syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Spastic paraplegia-severe developmental delay-epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Language delay and attention deficit-hyperactivity disorder/cognitive impairment Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Language delay and attention deficit-hyperactivity disorder/cognitive impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Short stature-brachydactyly-obesity-global developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Short stature-brachydactyly-obesity-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Expressive language delay Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Expressive language delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Motor delay Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Motor delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Growth delay due to insulin-like growth factor deficiency Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Growth delay due to insulin-like growth factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Neuromotor delay Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Neuromotor delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Pili torti-developmental delay-neurological abnormalities syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Pili torti-developmental delay-neurological abnormalities syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SEPHS1-related developmental delay Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SEPHS1-related developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

GRIN2B-related developmental delay Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the GRIN2B-related developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

alcohol-related neurodevelopmental disorder Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease alcohol-related neurodevelopmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

neurodevelopmental psychiatric disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neurodevelopmental psychiatric disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neurodevelopmental Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term neurodevelopmental in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

neurodevelopmental abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the neurodevelopmental abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

neurodevelopmental abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the neurodevelopmental abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Alcohol Related Neurodevelopmental Disorder Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Alcohol Related Neurodevelopmental Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Neurodevelopmental Disorder Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Neurodevelopmental Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Okur-Chung Neurodevelopmental Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Okur-Chung Neurodevelopmental Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Immunoskeletal Dysplasia With Neurodevelopmental Abnormalities Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Immunoskeletal Dysplasia With Neurodevelopmental Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Neurodevelopmental Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Neurodevelopmental Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Neurodevelopmental Abnormality Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Neurodevelopmental Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Gatad2B Associated Neurodevelopmental Disorder Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Gatad2B Associated Neurodevelopmental Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

alcohol-related neurodevelopmental disorder Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease alcohol-related neurodevelopmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with involuntary movements Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with involuntary movements in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Yoon-Bellen neurodevelopmental syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Yoon-Bellen neurodevelopmental syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with eye movement abnormalities and ataxia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with eye movement abnormalities and ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with speech impairment and dysmorphic facies Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with speech impairment and dysmorphic facies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with spasticity and poor growth Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with spasticity and poor growth in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Complex neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Complex neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

CACNA1A-related complex neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the CACNA1A-related complex neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

History of neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the History of neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Neurodevelopmental abnormality Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Neurodevelopmental abnormality phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

GNAO1-Related Neurodevelopmental Disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the GNAO1-Related Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

PPP2R1A-related neurodevelopmental disorders Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the PPP2R1A-related neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Syndromic complex neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Syndromic complex neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

STXBP1-associated neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the STXBP1-associated neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Neurodevelopmental Disability Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Neurodevelopmental Disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Okur-Chung neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Okur-Chung neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

NEURODEVELOPMENTAL DISOR Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the NEURODEVELOPMENTAL DISOR phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

TELO2-related intellectual disability-neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the TELO2-related intellectual disability-neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

DYNC1H1-related neurodevelopmental disorders Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the DYNC1H1-related neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

MBD5 associated neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the MBD5 associated neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SETD2 associated neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SETD2 associated neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

FAR1-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the FAR1-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Poirier-Bienvenu neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Poirier-Bienvenu neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SYT1-associated neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SYT1-associated neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

ARHGEF6-associated Neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the ARHGEF6-associated Neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SLC6A1-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SLC6A1-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Bryant-Li-Bhoj neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Bryant-Li-Bhoj neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Hiatt-Neu-Cooper neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hiatt-Neu-Cooper neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SLC9A7-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SLC9A7-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Syndromic neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Syndromic neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

ANK2-associated Neurodevelopmental Disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the ANK2-associated Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Focal segmental glomerulosclerosis and neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Focal segmental glomerulosclerosis and neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

UBR4-associated neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the UBR4-associated neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Neurodevelopmental disorder and structural brain anomalies Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Neurodevelopmental disorder and structural brain anomalies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Karayol-Borroto-Haghshenas neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Karayol-Borroto-Haghshenas neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SCN3A-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SCN3A-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

ARHGEF9-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the ARHGEF9-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Neurodevelopmental disorders Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

CDC42BPB-related neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the CDC42BPB-related neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Chilton-Okur-Chung neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Chilton-Okur-Chung neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Neurodevelopmental-craniofacial syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Neurodevelopmental-craniofacial syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

MORC2-related neurodevelopmental disorders Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the MORC2-related neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

TLK2-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the TLK2-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SETD2-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SETD2-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

PIGG-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the PIGG-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SCAMP5-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SCAMP5-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SCAMP5-related neurodevelopmental and movement disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SCAMP5-related neurodevelopmental and movement disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

ASH1L-related neurodevelopmental disorders Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the ASH1L-related neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

USP7-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the USP7-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Neurodevelopmental Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Neurodevelopmental phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

JMJD1C-associated Neurodevelopmental Disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the JMJD1C-associated Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SCN3A-related neurodevelopmental sisorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SCN3A-related neurodevelopmental sisorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

PAK1-related neurodevelopmental disorders Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the PAK1-related neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

CIC-related neurodevelopmental disorders Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the CIC-related neurodevelopmental disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

HIST1H1E-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the HIST1H1E-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

PLXNA1-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the PLXNA1-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Dworschak-Punetha neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Dworschak-Punetha neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

MTSS2-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the MTSS2-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

EZH1-neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the EZH1-neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

NRXN3-associated neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the NRXN3-associated neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

DHX34-related Neurodevelopmental Disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the DHX34-related Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SLC6A20-related Neurodevelopmental Disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SLC6A20-related Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

CACNA1D-related neurodevelopmental and endocrine disorders Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the CACNA1D-related neurodevelopmental and endocrine disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

TRRAP-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the TRRAP-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

WAC-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the WAC-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

TRAPPC6B-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the TRAPPC6B-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

CSNK2A1-related neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the CSNK2A1-related neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

KCND2-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the KCND2-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SNAP25 related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SNAP25 related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

CHRM1-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the CHRM1-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

PRKAR1B-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the PRKAR1B-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Marbach-Schaaf neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Marbach-Schaaf neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

PIP5K1C-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the PIP5K1C-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

CTR9-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the CTR9-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SCN8A-related complex neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SCN8A-related complex neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Parenti-mignot neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Parenti-mignot neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

DOHH related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the DOHH related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

AGO1-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the AGO1-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

CTCF-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the CTCF-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SPOP-related neurodevelopmental condition Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SPOP-related neurodevelopmental condition phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

USP9X-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the USP9X-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

GEMIN5-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the GEMIN5-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

NBEA-related complex neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the NBEA-related complex neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

DNHD1-related Neurodevelopmental Disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the DNHD1-related Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SLC4A10-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SLC4A10-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

JMJD1C-related Neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the JMJD1C-related Neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

ANK2-associated Complex Neurodevelopmental Disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the ANK2-associated Complex Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SYN1-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SYN1-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

TAOK2-associated neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the TAOK2-associated neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

EEF1D-associated Neurodevelopmental Syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the EEF1D-associated Neurodevelopmental Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

FBRSL1-associated neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the FBRSL1-associated neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

JARID2-related Neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the JARID2-related Neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

KIF21B-related Neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the KIF21B-related Neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

TAOK1-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the TAOK1-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SHANK1-related Neurodevelopmental Disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SHANK1-related Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SCAF4-associated Neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SCAF4-associated Neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

X-linked complex neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the X-linked complex neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

DNAH14-Associated Neurodevelopmental Disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the DNAH14-Associated Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

TOP2B-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the TOP2B-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

DDX23-related Neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the DDX23-related Neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

CNOT9-associated neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the CNOT9-associated neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

GPT2-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the GPT2-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

BAZ2B-associated neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the BAZ2B-associated neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

PAUL-CHAO NEURODEVELOPMENTAL SYNDR Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the PAUL-CHAO NEURODEVELOPMENTAL SYNDR phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Yoon-Bellen neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Yoon-Bellen neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple congenital anomalies-neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple congenital anomalies-neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Oculogastrointestinal-neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Oculogastrointestinal-neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

GRID1-associated neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the GRID1-associated neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Brunet-Wagner neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Brunet-Wagner neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Tessadori-van Haaften neurodevelopmental syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Tessadori-van Haaften neurodevelopmental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

UBR5-associated neurodevelopmental condition Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the UBR5-associated neurodevelopmental condition phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Childhood Onset VCP-related Neurodevelopmental Disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Childhood Onset VCP-related Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

CLDN5-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the CLDN5-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

SHANK1-associated neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the SHANK1-associated neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

RNU4-2-associated neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the RNU4-2-associated neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

El Hayek-Chahrour neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the El Hayek-Chahrour neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

KDM2A-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the KDM2A-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

UNC79-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the UNC79-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

GABBR1-related neurodevelopmental disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the GABBR1-related neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

PSMC5-related Neurodevelopmental proteasomopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the PSMC5-related Neurodevelopmental proteasomopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.