Disease association ontology term - MONDO:0011006 - hereditary spastic paraplegia 9A
Term summary
ID
MONDO:0011006
Name
hereditary spastic paraplegia 9A
Ontology or CV name
Disease association
Parents
is_a
autosomal dominant spastic paraplegia type 9
Annotation
Disease association
MONDO:0011006
-
hereditary spastic paraplegia 9A
References:
PB_REF:0000006
Genes:
pro1 (SPAC821.11)
pro2 (SPAC17H9.13c)