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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Ho Kaufman Mcalister Syndrome
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Accession:DOID:9001442 term browser browse the term
Synonyms:primary_id: MESH:C538325;   RDO:0004288
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 17251
    syndrome 8148
      Ho Kaufman Mcalister Syndrome 0
Path 2
Term Annotations click to browse term
  disease 17251
    Developmental Disease 10960
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9494
        Congenital Abnormalities 5594
          Musculoskeletal Abnormalities 2240
            Craniofacial Abnormalities 1961
              Maxillofacial Abnormalities 243
                Jaw Abnormalities 231
                  orofacial cleft 129
                    cleft palate 95
                      Ho Kaufman Mcalister Syndrome 0
paths to the root