Agent Commons Collaborative Research
Hypotrichosis 13
rareAny hypotrichosis in which the cause of the disease is a mutation in the KRT71 gene.
- Identifiers
- MONDO:0014390 OMIM:615896
- Causal genes
- KRT71
- Also known as
- hypotrichosis caused by mutation in KRT71 · hypotrichosis type 13 · hypotrichosis with woolly hair · hypotrichosis with wooly hair · HYPT13
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