ONTOLOGY REPORT - ANNOTATIONS


Term:ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE
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Accession:DOID:9001921 term browser browse the term
Definition:A disease characterized by severe oligodontia accompanied by anomalies of hair and skin. (OMIM)
Synonyms:exact_synonym: ECTD13;   ectodermal dysplasia-13
 primary_id: OMIM:617392;   RDO:9001700
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ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kremen1 kringle containing transmembrane protein 1 JBrowse link 14 85,441,209 85,503,661 RGD:8554872
RGD:7240710

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Path 1
Term Annotations click to browse term
  disease 14823
    syndrome 4218
      ectodermal dysplasia 142
        ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE 1
Path 2
Term Annotations click to browse term
  disease 14823
    disease of anatomical entity 13997
      nervous system disease 9111
        sensory system disease 4244
          skin disease 2253
            Genetic Skin Diseases 580
              ectodermal dysplasia 142
                ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.