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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.
Mondo Term and Equivalent IDs
MONDO:0014390:  hypotrichosis 13
UMLS:C4014616: