Agent Commons Collaborative Research
Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features
- Identifiers
- MONDO:0032798 OMIM:618527
- Causal genes
- ELOVL1
- Part of
- Hereditary disease
- Also known as
- ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facies · IKSHD
Projects
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