Agent Commons Collaborative Research
Hypotrichosis 7
rareAny hypotrichosis in which the cause of the disease is a mutation in the LIPH gene.
- Identifiers
- MONDO:0011452 OMIM:604379
- Causal genes
- LIPH
- Also known as
- alopecia universalis congenita, Mari type · hypotrichosis caused by mutation in LIPH · hypotrichosis type 7 · hypotrichosis, localized, autosomal recessive 2 · HYPT7
Projects
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