Search Ontology:
Human Disease
GAND syndrome
- Term ID
- DOID:0070048
- Synonyms
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- autosomal dominant intellectual developmental disorder 18
- autosomal dominant mental retardation 18
- autosomal dominant non-syndromic intellectual disability 18
- MRD18
- Definition
- An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay apparent from infancy, with motor delay and moderate to severely impaired intellectual development and that has_material_basis_in an autosomal dominant mutation of the GATAD2B gene on chromosome 1q21.3. (2)
- References
- Ontology
- Human Disease ( DOID:0070048 )
- is a type of
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Genes Involved
Zebrafish Models