Disease association ontology term - MONDO:0030935 - mitochondrial complex 2 deficiency, nuclear type 2

Term summary

ID: MONDO:0030935
Name: mitochondrial complex 2 deficiency, nuclear type 2
Ontology or CV name: Disease association

Parents

is_a mitochondrial complex II deficiency, nuclear type

Annotation

Disease association

MONDO:0030935 - mitochondrial complex 2 deficiency, nuclear type 2

References:

PB_REF:0000006

Genes:

sdh6 (SPAC664.12c)