nuclear type mitochondrial complex I deficiency 4

Term ID

DOID:0112082

Synonyms

MC1DN4

Definition

A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFV1 gene on chromosome 11q13.2. https://pubmed.ncbi.nlm.nih.gov/10080174/

References

OMIM:618225

Ontology

Human Disease ( DOID:0112082 )

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 Pages

Alliance (1)

Genes Involved

Zebrafish Models

Citations