Disease association ontology term - MONDO:0031019 - spastic paraplegia 87, autosomal recessive
Term summary
ID
MONDO:0031019
Name
spastic paraplegia 87, autosomal recessive
Ontology or CV name
Disease association
Parents
is_a
hereditary spastic paraplegia
Annotation
Disease association
MONDO:0031019
-
spastic paraplegia 87, autosomal recessive
References:
PB_REF:0000006
Genes:
rsn1 (SPBC354.08c)
SPAC24H6.13
SPAC2G11.09