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Disease Ontology Browser
hereditary spastic paraplegia 44 (DOID:0110796)
Synonyms: autosomal recessive spastic paraplegia 44; SPG44
Alt IDs: OMIM:613206, ICD10CM:G11.4, ORDO:320401
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the GJC2 gene on chromosome 1q42.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.08
The Jackson Laboratory