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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:Pachyonychia Congenita 3
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Accession:DOID:9000914 term browser browse the term
Synonyms:exact_synonym: PC3
 primary_id: OMIM:615726
For additional species annotation, visit the Alliance of Genome Resources.

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Pachyonychia Congenita 3 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Krt6a keratin 6A ISO OMIM NCBI chrNW_004936512:9,903,206...9,908,009 JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11994
    syndrome 5878
      ectodermal dysplasia 233
        pachyonychia congenita 1
          Pachyonychia Congenita 3 1
Path 2
Term Annotations click to browse term
  disease 11994
    Developmental Diseases 8574
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7550
        genetic disease 7134
          monogenic disease 5283
            autosomal genetic disease 4420
              autosomal dominant disease 2819
                pachyonychia congenita 1
                  Pachyonychia Congenita 3 1
paths to the root