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Disease Ontology Browser
hereditary spastic paraplegia 87 (DOID:0070456)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 87; SPG87
Alt IDs: OMIM:619966
Definition: A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM63C gene on chromosome 14q24.3.

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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last database update
MGI 6.23
The Jackson Laboratory