Non-Syndromic X-Linked Intellectual Disability 21
Disease ID: disease_node_16351
Connections displayed (default: 10).
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| Dbxref | MIM:300143 |
|---|---|
| Subclassof | DOID_0080012, DOID_0050776 |
| Data Source | DOID |
| Synonyms | MRX21, MRX34, X-linked mental retardation 21, X-linked mental retardation 21/34, X-linked mental retardation 34 |
| Doid Label | non-syndromic X-linked intellectual disability 21 |
| Doid Description | A non-syndromic X-linked intellectual disability characterized by a spectrum of cognitive neurologic impairments ranging from moderate mental retardation to high-functioning autism that has_material_basis_in hemizygous mutation in the IL1RAPL1 gene on chromosome Xp21.3-p21.2. |
| Has Material Basis In | GENO_0000149 |
| Disease Node Id | disease_node_16351 |
| Doid Id | DOID_0112022 |
| Label | Non-Syndromic X-Linked Intellectual Disability 21 |
- 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)