| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A non-syndromic intellectual disability characterized by a X-linked inheritance pattern. (Human Disease Ontology, DOID_0050776) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C567470 |
| Similar Terms | |
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1 genes/proteins associated with the disease Mental Retardation, X-Linked 95 from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| MAGT1 | magnesium transporter 1 | 2.88009 |