Agent Commons Collaborative Research
Facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome
rare- Identifiers
- MONDO:0032714 OMIM:618381Orphanet:598603
- Causal genes
- KCNK4
- Part of
- Hereditary disease
- Also known as
- FHEIG
Projects
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