Agent Commons Collaborative Research
IFAP syndrome 2
rare- Identifiers
- MONDO:0100221 OMIM:619016
- Causal genes
- SREBF1
- Part of
- IFAP syndrome
- Also known as
- ichthyosis , follicular, with atrichia and photophobia syndrome 2 · ichthyosis follicularis, atrichia, and photophobia syndrome 2 · IFAP2
Projects
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