Disease association ontology term - MONDO:0032617 - mitochondrial complex I deficiency, nuclear type 11

Term summary

ID: MONDO:0032617
Name: mitochondrial complex I deficiency, nuclear type 11
Ontology or CV name: Disease association

Parents

is_a mitochondrial complex I deficiency, nuclear type

Annotation

Disease association

MONDO:0032617 - mitochondrial complex I deficiency, nuclear type 11

References:

PB_REF:0000006

Genes:

SPAC9E9.15