Disease association ontology term - MONDO:0032626 - mitochondrial complex I deficiency, nuclear type 22

Term summary

ID: MONDO:0032626
Name: mitochondrial complex I deficiency, nuclear type 22
Ontology or CV name: Disease association

Parents

is_a mitochondrial complex I deficiency, nuclear type

Annotation

Disease association

MONDO:0032626 - mitochondrial complex I deficiency, nuclear type 22

References:

PB_REF:0000003

Genes:

cox16 (SPAC1486.08)