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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:SPOAN syndrome
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Accession:DOID:0060491 term browser browse the term
Definition:A neurodegenerative disease characterized by spastic paraplegia, axonal neuropathy, dysarthria, acoustic startle, and congenital optical atrophy and that has_material_basis_in homozygous mutation in the KLC2 gene on chromosome 11q13.2. (DO)
Synonyms:exact_synonym: spastic paraplegia, optic atrophy, and neuropathy;   spastic paraplegia, optic atrophy, and neuropathy syndrome;   spastic paraplegia, optic atropy, and neuropathy;   spastic paraplegia, optic atropy, and neuropathy syndrome
 primary_id: MESH:C563702
 alt_id: OMIM:609541;   RDO:0012893
 xref: ORDO:320406
For additional species annotation, visit the Alliance of Genome Resources.

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SPOAN syndrome term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Klc2 kinesin light chain 2 ISO ClinVar Annotator: match by term: SPOAN syndrome OMIM
PMID:24482476 PMID:25741868 PMID:26385635 PMID:28492532 NCBI chr 1:202,414,555...202,424,787
Ensembl chr 1:202,414,557...202,424,672
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18032
    syndrome 9456
      SPOAN syndrome 1
Path 2
Term Annotations click to browse term
  disease 18032
    disease of anatomical entity 17412
      nervous system disease 13079
        peripheral nervous system disease 2974
          neuropathy 2766
            cranial nerve disease 528
              optic nerve disease 282
                optic atrophy 176
                  SPOAN syndrome 1
paths to the root