ZFIN Human Disease: nuclear type mitochondrial complex I deficiency 11

OBO ID: DOID:0112089

Term Name:	nuclear type mitochondrial complex I deficiency 11		Search Ontology:
Synonyms:	MC1DN11
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF1 gene on chromosome 15q15.1. https://pubmed.ncbi.nlm.nih.gov/17557076/
References:	OMIM:618234
Ontology:	Human Disease ( DOID:0112089 )

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 11 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NDUFAF1	ndufaf1	Mitochondrial complex I deficiency, nuclear type 11	618234

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None