|
General Information
|
| Term |
Renpenning syndrome |
ID (Ontology) |
DOID:0060179 (Human Disease) |
| Definition |
An intellectual disability that is characterized by small head size (microcephaly), long narrow face, short stature, small testes, and intellectual deficit which follows X-linked inheritance and presents most often in males. |
| Also Known As |
"Golabi-Ito-Hall syndrome" ; "Sutherland-Haan X-linked mental retardation syndrome" ; "syndromic X-linked mental retardation 8" (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)
|
| Data Class | Field | Records |
|---|
|
| Alleles (FBal) | HUMAN_DISEASE_INTERACTIONS | 5 | | Human Disease Models (FBhh) | DOID | 1 |
|
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
| Full annotation statements | Relevant FlyBase reports |
|---|
| Alleles | Genes | Human Disease Models |
|---|
Renpenning syndrome | 5 | 4 | 1 | ameliorates | Renpenning syndrome | 2 | -- | -- | for disease ribbon | Renpenning syndrome | -- | 1 | -- | model of | Renpenning syndrome | 3 | 1 | -- |
|
Relationships