OBO ID: DOID:0080112
Term Name: mitochondrial complex III deficiency nuclear type 3 Search Ontology:
Synonyms:
Definition: A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCRB gene on chromosome 8q22. http://omim.org/entry/615158?search=615158&highlight=615158
References:
Ontology: Human Disease   ( DOID:0080112 )
OTHER mitochondrial complex III deficiency nuclear type 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
UQCRB Mitochondrial complex III deficiency, nuclear type 3 615158
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None