|
| General Information | |||
|---|---|---|---|
| Term | non-syndromic X-linked intellectual disability 53 | ID (Ontology) | DOID:0112047 (Human Disease) |
| Definition | A non-syndromic X-linked intellectual disability that has_material_basis_in hemizygous mutation in a region on chromosome Xq22.2-q26. | ||
| Also Known As | "MRX53" ; "X-linked mental retardation 53" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
X-linked monogenic disease |__non-syndromic X-linked intellectual disability__ |__X-linked recessive disease______________________| non-syndromic intellectual disability | |__non-syndromic X-linked intellectual disability__| non-syndromic X-linked intellectual disability 53 |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
non-syndromic X-linked intellectual disability X-linked recessive disease |
||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
| MIM:300324 | |||