Disease association ontology term - MONDO:0971149 - spastic paraplegia 30B, autosomal recessive
Term summary
ID
MONDO:0971149
Name
spastic paraplegia 30B, autosomal recessive
Ontology or CV name
Disease association
Parents
is_a
autosomal recessive disease
is_a
hereditary spastic paraplegia 30
Annotation
Disease association
MONDO:0971149
-
spastic paraplegia 30B, autosomal recessive
References:
PB_REF:0000006
Genes:
klp8 (SPAC144.14)