Autosomal Domit Intellectual Developmental Disorder 21
Disease ID: disease_node_16506
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| Dbxref | MIM:615502 |
|---|---|
| Subclassof | DOID_0060307 |
| Data Source | DOID |
| Synonyms | MRD21, autosomal dominant mental retardation 21, autosomal dominant non-syndromic intellectual disability 21 |
| Doid Label | autosomal domit intellectual developmental disorder 21 |
| Doid Description | An autosomal domit intellectual developmental disorder that has_material_basis_in an autosomal domit mutation of the CTCF gene on chromosome 16q22.1. |
| Disease Node Id | disease_node_16506 |
| Doid Id | DOID_0070051 |
| Label | Autosomal Domit Intellectual Developmental Disorder 21 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Intellectual Developmental Disorder(ID:disease_node_16455) (Disease)