ZFIN Human Disease: nuclear type mitochondrial complex I deficiency 3

OBO ID: DOID:0112093

Term Name:	nuclear type mitochondrial complex I deficiency 3		Search Ontology:
Synonyms:	MC1DN3
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS7 gene on chromosome 19p13.3. (2)
References:	OMIM:618224
Ontology:	Human Disease ( DOID:0112093 )

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 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NDUFS7	ndufs7	Mitochondrial complex I deficiency, nuclear type 3	618224

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None