Non-Syndromic X-Linked Intellectual Disability 101
Disease ID: disease_node_16327
Connections displayed (default: 10).
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| Dbxref | MIM:300928 |
|---|---|
| Subclassof | DOID_0080012, DOID_0050776 |
| Data Source | DOID |
| Synonyms | MRX101, X-linked mental retardation 101 |
| Doid Label | non-syndromic X-linked intellectual disability 101 |
| Doid Description | A non-syndromic X-linked intellectual disability characterized by global developmental delay that has_material_basis_in hemizygous mutation in the MID2 gene on chromosome Xq22.3. |
| Has Material Basis In | GENO_0000149 |
| Disease Node Id | disease_node_16327 |
| Doid Id | DOID_0112048 |
| Label | Non-Syndromic X-Linked Intellectual Disability 101 |
- Outgoing r'ship
SUBCLASS_OFto/from Non-Syndromic X-Linked Intellectual Disability(ID:disease_node_16316) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from X-Linked Recessive Disease(ID:disease_node_13254) (Disease)