|
General Information
|
| Term |
non-syndromic X-linked intellectual disability 50 |
ID (Ontology) |
DOID:0112029 (Human Disease) |
| Definition |
A non-syndromic X-linked intellectual disability characterized by moderate intellectual disability that has_material_basis_in mutation in a region on chromosome Xp11.3-p11.21. |
| Also Known As |
"MRX50" ; "X-linked intellectual developmental disorder 50" ; "X-linked mental retardation 50" (for all, see Synonyms field below) |
| Comment |
|
|
Links to External Ontologies
|
|
DO.org
|
|
Annotations
|
|
Records annotated with this term OR any of its CHILD TERMS
|
|
|
|
Records annotated with this exact term (annotations to child terms are NOT included)
|
|
No relevant records available
|
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
| Full annotation statements | Relevant FlyBase reports |
|---|
| Genes |
|---|
non-syndromic X-linked intellectual disability 50 | 1 | for disease ribbon | non-syndromic X-linked intellectual disability 50 | 1 | model of | non-syndromic X-linked intellectual disability 50 | 1 |
|
Relationships