ZFIN Human Disease: nuclear type mitochondrial complex I deficiency 26

OBO ID: DOID:0112086

Term Name:	nuclear type mitochondrial complex I deficiency 26		Search Ontology:
Synonyms:	MC1DN26
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA9 gene on chromosome 12p13.32. https://pubmed.ncbi.nlm.nih.gov/22114105/
References:	OMIM:618247
Ontology:	Human Disease ( DOID:0112086 )

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 26 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NDUFA9	ndufa9a ndufa9b	Mitochondrial complex I deficiency, nuclear type 26	618247

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None