Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language

Preferred Label : Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language;

Symbol : NEDTCHAL;

Type : Phenotype, molecular basis known;

Prefixed ID : #621150;

Details

Origin ID

621150;

Genes related to phenotype
- Eukaryotic translation elongation factor 1, delta [OMIM gene]

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