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Download Data for alopecia universalis congenita
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
This disease has been annotated by GARD as a rare disease.
Description from Mondo Disease Ontology.
Description from UniProt.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0050634
GARD:0000614
MESH:C537055
OMIM:203655
Orphanet:701
SCTID:86166000
UMLS:C0263505
MONDO:0008757
High level summary of knowledge for a disease, including descriptions and datasource references.
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Opens the Target List with this set of targets