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Human Disease
neurodevelopmental disorder with dysmorphic facies and thin corpus callosum
- Term ID
- DOID:0070469
- Synonyms
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- NEDDFAC
- Definition
- An autosomal dominant intellectual developmental disorder characterized by global developmental delay, impaired intellectual development with poor or absent speech and language, dysmorphic facial features, and corpus callosum abnormalities that has_material_basis_in heterozygous mutation in the SUPT16H gene on chromosome 14q11.2. (2)
- References
- Ontology
- Human Disease ( DOID:0070469 )
- is a type of
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Zebrafish Models