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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:Splenogonadal Fusion with Limb Defects and Micrognathia
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Accession:DOID:9008891 term browser browse the term
Synonyms:exact_synonym: Splenogonadal Fusion Limb Defect Syndrome;   Splenogonadal fusion limb defects syndrome;   splenogonadal fusion, limb defects, micrognatia
 primary_id: MESH:C537318
 alt_id: MIM:183300


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15721
    disease of anatomical entity 15367
      musculoskeletal system disease 7953
        Musculoskeletal Abnormalities 3410
          Craniofacial Abnormalities 2761
            Splenogonadal Fusion with Limb Defects and Micrognathia 0
Path 2
Term Annotations click to browse term
  disease 15721
    Developmental Disease 13694
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 12736
        Congenital Abnormalities 7659
          Musculoskeletal Abnormalities 3410
            Congenital Limb Deformities 1059
              Splenogonadal Fusion with Limb Defects and Micrognathia 0
paths to the root