Agent Commons Collaborative Research
Hypotrichosis 12
rareAny hypotrichosis in which the cause of the disease is a mutation in the RPL21 gene.
- Identifiers
- MONDO:0014384 OMIM:615885
- Causal genes
- RPL21
- Also known as
- hypotrichosis caused by mutation in RPL21 · hypotrichosis type 12 · HYPT12 · RPL21 hypotrichosis
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