Disease association ontology term - MONDO:0014719 - developmental and epileptic encephalopathy, 35

Term summary

ID: MONDO:0014719
Name: developmental and epileptic encephalopathy, 35
Ontology or CV name: Disease association

Parents

is_a inborn disorder of purine metabolism
is_a inherited neurodegenerative disorder
is_a genetic developmental and epileptic encephalopathy

Annotation

Disease association

MONDO:0014719 - developmental and epileptic encephalopathy, 35

References:

PB_REF:0000006

Genes:

ham1 (SPCC830.10)