ZFIN Human Disease: nuclear type mitochondrial complex I deficiency 22

OBO ID: DOID:0112069

Term Name:	nuclear type mitochondrial complex I deficiency 22		Search Ontology:
Synonyms:	MC1DN22
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA10 gene on chromosome 2q37.3. https://pubmed.ncbi.nlm.nih.gov/21150889/
References:	OMIM:618243
Ontology:	Human Disease ( DOID:0112069 )

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 22 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NDUFA10	ndufa10	Mitochondrial complex I deficiency, nuclear type 22	618243

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None