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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.
Mondo Term and Equivalent IDs
MONDO:0007806:  hypotrichosis 4
MESH:C567718: 
UMLS:C2750815: