Term Name: hereditary spastic paraplegia 18B
Synonyms: spastic paraplegia 18B
Definition: A hereditary spastic paraplegia 18 that has_material_basis_in homozygous mutation in the ERLIN2 gene on chromosome 8p11.
Ontology: Human Disease [DOID:0070641]   ( DOID:0070641 )

Relationships
is a type of: autosomal recessive disease hereditary spastic paraplegia 18