Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Developmental Disabilities | | ISO | FOXP4 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Global developmental delay | ClinVar | | genetic disease | | ISO | FOXP4 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | infantile Refsum disease | | ISO | FOXP4 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: ADRENOLEUKODYSTROPHY and AUTOSOMAL NEONATAL | ClinVar | PMID:19877282 more ... | lung adenocarcinoma | | ISO | FOXP4 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Lung adenocarcinoma | ClinVar | PMID:27993330 | sensorineural hearing loss | | ISO | FOXP4 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sensorineural hearing loss disorder | ClinVar | PMID:25741868 and PMID:28492532 | Zellweger syndrome | | ISO | FOXP4 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Peroxisome biogenesis disorders and Zellweger syndrome spectrum | ClinVar | PMID:19877282 more ... | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Imported Disease Annotations - CTD
Gene Ontology Annotations Click to see Annotation Detail View
Biological Process
Cellular Component
Molecular Function
