autosomal recessive sensory neuropathy with spastic paraplegia Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive sensory neuropathy with spastic paraplegia (DOID:0061188)
Alliance: disease page
Alt IDs: OMIM:256840, MESH:C564948, ORDO:139578, UMLS_CUI:C1850395, UMLS_CUI:C5679610
Definition: A hereditary sensory and autonomic neuropathy that has_material_basis_in homozygous mutation in the CCT5 gene on chromosome 5p15.2.

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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