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Disease Ontology Term: mitochondrial complex V (ATP synthase) deficiency nuclear type 7

DO ID
DOID:0070464
Description
A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the ATP5PO gene on chromosome 21q22.11.
Synonyms
MC5DN7
View DO Annotations for yeast and other model organisms at the Alliance of Genome Resources

Ontology Diagram

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Annotations

Manually Curated

There are no manually curated annotations for mitochondrial complex V (ATP synthase) deficiency nuclear type 7.

High-throughput

There are no high-throughput annotations for mitochondrial complex V (ATP synthase) deficiency nuclear type 7.

Computational

There are no computational annotations for mitochondrial complex V (ATP synthase) deficiency nuclear type 7.
genetic disease (0)