mitochondrial complex III deficiency nuclear type 4

Go to external page http://purl.obolibrary.org/obo/DOID_0080113


A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCRQ gene on chromosome 5q31. [ url:http://omim.org/entry/615159?search=615159&highlight=615159 http://purl.obolibrary.org/obo/ECO_0007636 ]

This is just here as a test because I lose it

Term information

has obo namespace

disease_ontology

id

DOID:0080113