Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination (Q69633053)
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rare genetic disease
- Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination |
rare genetic disease |
|
Statements
3 references
Identifiers
1 reference