Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
|
| gptkbp:affects |
females
|
| gptkbp:causedBy |
mutation in MECP2 gene
|
| gptkbp:class |
gptkb:autism_spectrum_disorder
neurological disorder |
| gptkbp:firstDescribed |
1966
|
| gptkbp:frequency |
rare
|
| https://www.w3.org/2000/01/rdf-schema#label |
F84.2 Rett syndrome
|
| gptkbp:ICD-10_code |
F84.2
|
| gptkbp:namedAfter |
gptkb:Andreas_Rett
|
| gptkbp:onset |
early childhood
|
| gptkbp:prognosis |
progressive
|
| gptkbp:symptom |
intellectual disability
gait abnormalities loss of purposeful hand skills impaired language development stereotypic hand movements |
| gptkbp:treatment |
supportive care
occupational therapy physical therapy speech therapy |
| gptkbp:bfsParent |
gptkb:F84_Pervasive_developmental_disorders
|
| gptkbp:bfsLayer |
7
|