ZFIN Human Disease: nuclear type mitochondrial complex I deficiency 9

OBO ID: DOID:0112073

Term Name:	nuclear type mitochondrial complex I deficiency 9		Search Ontology:
Synonyms:	MC1DN9
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS6 gene on chromosome 5p15.33. https://pubmed.ncbi.nlm.nih.gov/15372108/
References:	OMIM:618232
Ontology:	Human Disease ( DOID:0112073 )

Relationships

is a type of:	autosomal recessive disease nuclear type mitochondrial complex I deficiency autosomal recessive disease nuclear type mitochondrial complex I deficiency Show first 5 Terms

OTHER nuclear type mitochondrial complex I deficiency 9 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NDUFS6	ndufs6	Mitochondrial complex I deficiency, nuclear type 9	618232

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None