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ONTOLOGY REPORT - ANNOTATIONS


Term:Kindler syndrome
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Accession:DOID:0060472 term browser browse the term
Definition:A skin disease characterized by congenital blistering, skin atrophy, photosensitivity, skin fragility, and scaling. (DO)
Synonyms:exact_synonym: Bullous acrokeratotic poikiloderma of kindler and weary;   Congenital bullous poikiloderma;   KNDLRS;   Kindler's syndrome;   Poikiloderma, congenital, with bullae, weary type;   Poikiloderma, hereditary acrokeratotic;   hereditary acrokeratotic poikiloderma of Kindler-Weary;   poikiloderma of Kindler
 primary_id: MESH:C536321
 alt_id: OMIM:173650;   RDO:0001857
 xref: GARD:4391;   ORDO:306539
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Kindler syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fermt1 fermitin family member 1 JBrowse link NW_004936485 12,985,552 13,016,997 RGD:7240710
RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11368
    Stomatognathic Diseases 790
      tooth disease 211
        periodontal disease 89
          Kindler syndrome 1
Path 2
Term Annotations click to browse term
  disease 11368
    disease of anatomical entity 11036
      nervous system disease 8876
        sensory system disease 4180
          skin disease 2166
            vesiculobullous skin disease 101
              epidermolysis bullosa 48
                Kindler syndrome 1
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.