|
General Information
|
| Term |
mitochondrial complex V (ATP synthase) deficiency nuclear type 4A |
ID (Ontology) |
DOID:0070461 (Human Disease) |
| Definition |
A mitochondrial complex V (ATP synthase) deficiency nuclear type 4 characterized by infantile onset of poor feeding and failure to thrive that may resolve spontaneously or progress to include developmental delay with impaired intellectual development and movement abnormalities that has_material_basis_in autosomal dominant inheritance. |
| Also Known As |
"MC5DN4A" |
| 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 |
|---|
mitochondrial complex V (ATP synthase) deficiency nuclear type 4A | 1 | for disease ribbon | mitochondrial complex V (ATP synthase) deficiency nuclear type 4A | 1 | model of | mitochondrial complex V (ATP synthase) deficiency nuclear type 4A | 1 |
|
Relationships