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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 2 132,904,177 132,946,036 RGD:8554872
RGD:13592920
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12526
    Stomatognathic Diseases 844
      tooth disease 229
        periodontal disease 100
          Kindler syndrome 1
Path 2
Term Annotations click to browse term
  disease 12526
    disease of anatomical entity 12146
      nervous system disease 9643
        sensory system disease 4458
          skin disease 2325
            vesiculobullous skin disease 111
              epidermolysis bullosa 49
                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.