Mental Retardation, X-linked
GPTKB entity
Statements (18)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:genetic_disorder
|
| gptkbp:affects |
cognitive development
males more than females |
| gptkbp:alsoKnownAs |
gptkb:X-linked_intellectual_disability
|
| gptkbp:category |
gptkb:neurological_disorder
X-linked recessive disease |
| gptkbp:causedBy |
mutations in various X-linked genes
|
| gptkbp:diagnosedBy |
genetic testing
|
| gptkbp:firstDescribed |
1943
|
| gptkbp:inheritance |
X-linked
|
| gptkbp:OMIM |
300000
|
| gptkbp:prevalence |
rare
|
| gptkbp:symptom |
gptkb:intellectual_disability
developmental delay |
| gptkbp:treatment |
supportive care
|
| gptkbp:bfsParent |
gptkb:MRX
|
| gptkbp:bfsLayer |
8
|
| https://www.w3.org/2000/01/rdf-schema#label |
Mental Retardation, X-linked
|