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ONTOLOGY REPORT - ANNOTATIONS


Term:Multiple Epiphyseal Dysplasia with Robin Phenotype
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Accession:DOID:9001369 term browser browse the term
Synonyms:primary_id: MESH:C563291
 alt_id: RDO:0012596
For additional species annotation, visit the Alliance of Genome Resources.


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15599
    physical disorder 738
      orofacial cleft 114
        cleft palate 92
          Multiple Epiphyseal Dysplasia with Robin Phenotype 0
Path 2
Term Annotations click to browse term
  disease 15599
    Developmental Diseases 8726
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7507
        Congenital Abnormalities 3579
          Musculoskeletal Abnormalities 1296
            Craniofacial Abnormalities 1040
              Maxillofacial Abnormalities 207
                Jaw Abnormalities 204
                  orofacial cleft 114
                    cleft palate 92
                      Multiple Epiphyseal Dysplasia with Robin Phenotype 0
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.