Autosomal Domit Intellectual Developmental Disorder 39
Disease ID: disease_node_16488
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:616521 |
|---|---|
| Subclassof | DOID_0060307 |
| Data Source | DOID |
| Synonyms | MRD39, autosomal dominant mental retardation 39, autosomal dominant non-syndromic intellectual disability 39 |
| Doid Label | autosomal domit intellectual developmental disorder 39 |
| Doid Description | An autosomal domit intellectual developmental disorder that has_material_basis_in an autosomal domit heterozygous mutation in the MYT1L gene on chromosome 2p25.3. |
| Disease Node Id | disease_node_16488 |
| Doid Id | DOID_0070069 |
| Label | Autosomal Domit Intellectual Developmental Disorder 39 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Intellectual Developmental Disorder(ID:disease_node_16455) (Disease)