ZFIN Human Disease: nuclear type mitochondrial complex I deficiency 25

OBO ID: DOID:0112067

Term Name:	nuclear type mitochondrial complex I deficiency 25		Search Ontology:
Synonyms:	MC1DN25
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous and compound heterozygous mutation in the NDUFB3 gene on chromosome 2q33.1. https://pubmed.ncbi.nlm.nih.gov/22277967/
References:	OMIM:618246
Ontology:	Human Disease ( DOID:0112067 )

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 25 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NDUFB3	ndufb3	Mitochondrial complex I deficiency, nuclear type 25	618246

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None