ZFIN Human Disease: nuclear type mitochondrial complex I deficiency 24

OBO ID: DOID:0112079

Term Name:	nuclear type mitochondrial complex I deficiency 24		Search Ontology:
Synonyms:	MC1DN24
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFB9 gene on chromosome 8q24.13. https://pubmed.ncbi.nlm.nih.gov/22200994/
References:	OMIM:618245
Ontology:	Human Disease ( DOID:0112079 )

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 24 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NDUFB9	ndufb9	?Mitochondrial complex I deficiency, nuclear type 24	618245

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None