Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | genetic disease | | ISO | XPO5 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | infantile Refsum disease | | ISO | XPO5 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: ADRENOLEUKODYSTROPHY and AUTOSOMAL NEONATAL | ClinVar | PMID:19877282 more ... | Zellweger syndrome | | ISO | XPO5 (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-Chemical Interaction Annotations Click to see Annotation Detail View
Gene Ontology Annotations Click to see Annotation Detail View
Biological Process
Cellular Component
Molecular Function
Molecular Pathway Annotations Click to see Annotation Detail View
