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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.
Mondo Term and Equivalent IDs
MONDO:0013514:  hypotrichosis 3
UMLS:C3151432: