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hypotrichosis 3
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any hypotrichosis in which the cause of the disease is a mutation in the KRT74 gene.
Uniprot Description A condition characterized by the presence of less than the normal amount of hair. Affected individuals have normal hair in early childhood but experience progressive hair loss limited to the scalp beginning in the middle of the first decade and almost complete baldness by the third decade. Body hair, beard, eyebrows, axillary hair, teeth, and nails develop normally.
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:0110700
OMIM:613981
UMLS:C3151432
MONDO:0013514
High level summary of knowledge for a disease, including descriptions and datasource references.