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hypotrichosis 1
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any hypotrichosis in which the cause of the disease is a mutation in the APCDD1 gene.
Uniprot Description A rare form of non-syndromic hereditary hypotrichosis without characteristic hair shaft anomalies. Affected individuals typically show normal hair at birth, but hair loss and thinning of the hair shaft start during early childhood and progress with age.
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.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0110698
OMIM:605389
MONDO:0011549
High level summary of knowledge for a disease, including descriptions and datasource references.