hereditary spastic paraplegia 18A Disease Ontology Browser

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hereditary spastic paraplegia 18A (DOID:0070640)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 18; spastic paraplegia 18A
Alt IDs: OMIM:620512
Definition: A hereditary spastic paraplegia 18 that has_material_basis_in heterozygous mutation in the ERLIN2 gene on chromosome 8p11.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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