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ONTOLOGY REPORT - ANNOTATIONS


Term:hereditary spastic paraplegia 15
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Accession:DOID:0110768 term browser browse the term
Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE26 gene on chromosome 14q24.1. (DO)
Synonyms:exact_synonym: Kjellin syndrome;   SPG15;   autosomal recessive spastic paraplegia 15;   autosomal recessive spastic paraplegia type 15;   hereditary spastic paraparesis type 15;   recessive spastic paraplegia with retinal degeneration;   spastic paraplegia 15;   spastic paraplegia and retinal degeneration;   spastic paraplegia-retinal degeneration syndrome
 primary_id: MESH:C536642
 alt_id: OMIM:270700;   RDO:0002282
 xref: GARD:9581;   ORDO:100996
For additional species annotation, visit the Alliance of Genome Resources.


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hereditary spastic paraplegia 15 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Zfyve26 zinc finger FYVE-type containing 26 JBrowse link 6 102,409,235 102,472,962 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15849
    sensory system disease 4942
      eye disease 2378
        eye degenerative disease 444
          retinal degeneration 442
            hereditary spastic paraplegia 15 1
Path 2
Term Annotations click to browse term
  disease 15849
    disease of anatomical entity 15241
      nervous system disease 10711
        central nervous system disease 8827
          neurodegenerative disease 3133
            Nervous System Heredodegenerative Disorders 1901
              motor peripheral neuropathy 520
                hereditary spastic paraplegia 131
                  hereditary spastic paraplegia 15 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.