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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) 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:Brachytelephalangy Characteristic Facies Kallmann
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Accession:DOID:9002617 term browser browse the term
Synonyms:exact_synonym: Brachytelephalangy with Characteristic Facies and Kallmann Syndrome;   Characteristic craniofacial appearance and brachytelephalangy
 primary_id: MESH:C537101
 alt_id: MIM:113480


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19150
    syndrome 11436
      Kallmann syndrome 35
        Brachytelephalangy Characteristic Facies Kallmann 0
Path 2
Term Annotations click to browse term
  disease 19150
    Developmental Disease 14694
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 13756
        Congenital Abnormalities 7973
          Urogenital Abnormalities 464
            disorder of sexual development 240
              46, XY Disorders of Sex Development 85
                Kallmann syndrome 35
                  Brachytelephalangy Characteristic Facies Kallmann 0
paths to the root