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hypotrichosis
Disease Summary
Associated Targets (40)
Tbio
32
Tchem
6
Tclin
2
Mondo Description A congenital condition, usually due to genetic aberrations, that is characterized by a lack of hair growth on the head and/or body.
Disease Ontology Description A hair disease that is characterized by sparse hair on the scalp resulting from abnormal hair follicle development and has_material_basis in mutations in proteins involved in hair growth, division or proliferation of cells within hair follicles.
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 Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:4535
MESH:D007039
NCIT:C34720
OMIMPS:605389
SCTID:53602002
MONDO:0003037
High level summary of knowledge for a disease, including descriptions and datasource references.