Autosomal Domit Intellectual Developmental Disorder 38
Disease ID: disease_node_16489
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| Dbxref | MIM:616393 |
|---|---|
| Subclassof | DOID_0060307 |
| Data Source | DOID |
| Synonyms | MRD38, PRELDS, autosomal dominant mental retardation 38, autosomal dominant non-syndromic intellectual disability 38, psychomotor retardation, epilepsy, and language disability syndrome |
| Doid Label | autosomal domit intellectual developmental disorder 38 |
| Doid Description | An autosomal domit intellectual developmental disorder that has_material_basis_in an autosomal domit mutation of the EEF1A2 gene on chromosome 20q13.33. |
| Disease Node Id | disease_node_16489 |
| Doid Id | DOID_0070068 |
| Label | Autosomal Domit Intellectual Developmental Disorder 38 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Intellectual Developmental Disorder(ID:disease_node_16455) (Disease)