Search Ontology:

Human Disease

mitochondrial complex V (ATP synthase) deficiency nuclear type 4

Term ID

DOID:0060333

Synonyms

MC5DN4

Definition

A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in mutation in the ATP5F1A gene on chromosome 18q21.1. (2)

References

Ontology

Human Disease ( DOID:0060333 )

Relationships

is a type of: mitochondrial complex V (ATP synthase) deficiency

mitochondrial complex V (ATP synthase) deficiency Show first 5 Terms
has subtype: mitochondrial complex V (ATP synthase) deficiency nuclear type 4A mitochondrial complex V (ATP synthase) deficiency nuclear type 4B

mitochondrial complex V (ATP synthase) deficiency nuclear type 4A mitochondrial complex V (ATP synthase) deficiency nuclear type 4B Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models