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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:Postaxial Polydactyly, Type A8
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Accession:DOID:9008857 term browser browse the term
Definition:A disease characterized by the presence of postaxial extra digits (hexadactyly) on the hands and/or the feet. The anomalous digits are well formed and have nails. PAPA8 is caused by homozygous mutation in the GLI1 gene on chromosome 12q13. (OMIM)
Synonyms:exact_synonym: PAPA8
 primary_id: OMIM:618123
For additional species annotation, visit the Alliance of Genome Resources.


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Postaxial Polydactyly, Type A8 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Gli1 GLI-Kruppel family member GLI1 ISO ClinVar Annotator: match by term: POLYDACTYLY, POSTAXIAL, TYPE A8 ClinVar
OMIM
PMID:25741868 PMID:28973407 NCBI chr10:127,329,882...127,341,579
Ensembl chr10:127,329,882...127,341,974
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14453
    physical disorder 3096
      polydactyly 118
        Postaxial Polydactyly 12
          Postaxial Polydactyly, Type A8 1
Path 2
Term Annotations click to browse term
  disease 14453
    Developmental Disease 10779
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9290
        Congenital Abnormalities 5601
          Musculoskeletal Abnormalities 2255
            Congenital Limb Deformities 452
              polydactyly 118
                Postaxial Polydactyly 12
                  Postaxial Polydactyly, Type A8 1
paths to the root