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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:orofacial cleft 6
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Accession:DOID:0080593 term browser browse the term
Definition:An orofacial cleft that has_material_basis_in variation in an enhancer of the IRF6 gene on chromosome 1q32. (DO)
Synonyms:exact_synonym: OFC6
 related_synonym: nonsyndromic cleft lip with or without cleft palate 6;   orofacial cleft 6, susceptibility to
 primary_id: OMIM:608864
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 17286
    physical disorder 3106
      orofacial cleft 130
        orofacial cleft 6 1
Path 2
Term Annotations click to browse term
  disease 17286
    Developmental Disease 10988
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9531
        Congenital Abnormalities 5606
          Musculoskeletal Abnormalities 2245
            Craniofacial Abnormalities 1966
              Maxillofacial Abnormalities 244
                Jaw Abnormalities 232
                  orofacial cleft 130
                    orofacial cleft 6 1
paths to the root