Disease association ontology term - MONDO:0032631 - mitochondrial complex I deficiency, nuclear type 27

Term summary

ID: MONDO:0032631
Name: mitochondrial complex I deficiency, nuclear type 27
Ontology or CV name: Disease association

Parents

is_a mitochondrial complex I deficiency, nuclear type

Annotation

Disease association

MONDO:0032631 - mitochondrial complex I deficiency, nuclear type 27

References:

PB_REF:0000006

Genes:

fmt1 (SPAC1805.09c)