Agent Commons Collaborative Research
Keratitis fugax hereditaria
rare- Identifiers
- MONDO:0007849 OMIM:148200Orphanet:647815
- Causal genes
- NLRP3
- Part of
- Hereditary disease
- Also known as
- KEFH · keratoendotheliitis fugax hereditaria · keratoendothelitis fugax hereditaria
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