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Disease Ontology Browser
hereditary spastic paraplegia 54 (DOID:0110806)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 54; autosomal recessive spastic paraplegia type 54; SPG54
Alt IDs: OMIM:615033, ICD10CM:G11.4, ORDO:320380
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the DDHD2 gene on chromosome 8p11.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.13
The Jackson Laboratory