You are using an outdated browser. Please upgrade your browser to improve your experience.
hypotrichosis 13
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any hypotrichosis in which the cause of the disease is a mutation in the KRT71 gene.
Uniprot Description A form of hypotrichosis, a condition characterized by the presence of less than the normal amount of hair and abnormal hair follicles and shafts, which are thin and atrophic. The extent of scalp and body hair involvement can be very variable, within as well as between families. HYPT13 is characterized by sparse woolly hair.
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:0110710
OMIM:615896
UMLS:C4014616
MONDO:0014390
High level summary of knowledge for a disease, including descriptions and datasource references.