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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
For additional species annotation, visit the Alliance of Genome Resources.


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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_004955415 16,447,921 16,483,221 RGD:7240710
RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11242
    Stomatognathic Diseases 793
      tooth disease 210
        periodontal disease 86
          Kindler syndrome 1
Path 2
Term Annotations click to browse term
  disease 11242
    disease of anatomical entity 10909
      nervous system disease 8758
        sensory system disease 4123
          skin disease 2128
            vesiculobullous skin disease 102
              epidermolysis bullosa 47
                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.