Gand Syndrome
Disease ID: disease_node_16509
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| Dbxref | MIM:615074 |
|---|---|
| Subclassof | DOID_0060307 |
| Data Source | DOID |
| Synonyms | MRD18, autosomal dominant intellectual developmental disorder 18, autosomal dominant mental retardation 18, autosomal dominant non-syndromic intellectual disability 18 |
| Doid Label | GAND syndrome |
| Doid Description | An autosomal domit 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 domit mutation of the GATAD2B gene on chromosome 1q21.3. |
| Disease Node Id | disease_node_16509 |
| Doid Id | DOID_0070048 |
| Label | Gand Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Intellectual Developmental Disorder(ID:disease_node_16455) (Disease)