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hypotrichosis 4
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any hypotrichosis in which the cause of the disease is a mutation in the HR gene.
Uniprot Description An autosomal dominant condition characterized by reduced amount of hair, alopecia, little or no eyebrows, eyelashes or body hair, and coarse, wiry, twisted hair in early childhood.
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:0110701
MESH:C567718
OMIM:146550
UMLS:C2750815
MONDO:0007806
High level summary of knowledge for a disease, including descriptions and datasource references.