Disease association ontology term - MONDO:0014567 - glutamate pyruvate transaminase 2 deficiency

Term summary

ID: MONDO:0014567
Name: glutamate pyruvate transaminase 2 deficiency
Ontology or CV name: Disease association

Parents

excluded_subClassOf syndromic intellectual disability
is_a complex hereditary spastic paraplegia

Annotation

Disease association

MONDO:0014567 - glutamate pyruvate transaminase 2 deficiency

References:

PB_REF:0000006

Genes:

alt1 (SPBC582.08)