Autosomal Domit Intellectual Developmental Disorder 19
Disease ID: disease_node_16508
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| Dbxref | MIM:615075 |
|---|---|
| Subclassof | DOID_0060307 |
| Data Source | DOID |
| Synonyms | MRD19, autosomal dominant mental retardation 19, autosomal dominant non-syndromic intellectual disability 19 |
| Doid Label | autosomal domit intellectual developmental disorder 19 |
| Doid Description | An autosomal domit intellectual developmental disorder that has_material_basis_in an autosomal domit mutation of the CTNNB1 gene on chromosome 3p22.1. |
| Disease Node Id | disease_node_16508 |
| Doid Id | DOID_0070049 |
| Label | Autosomal Domit Intellectual Developmental Disorder 19 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Intellectual Developmental Disorder(ID:disease_node_16455) (Disease)