Send us a Message

Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   


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.

go back to main search page
Accession:DOID:0080038 term browser browse the term
Definition:An osteochondrodysplasia that has_material_basis_in a mutation in the CTSK gene which results_in dwarfism, brittle bones, osteopetrosis, shortening of the distal phalanges. (DO)
Synonyms:exact_synonym: PKND;   PYCD;   pycnodysostoses;   pyknodysostoses;   pyknodysostosis
 primary_id: MESH:D058631
 alt_id: OMIM:265800
 xref: GARD:4611;   ORDO:763
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
pycnodysostosis term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ctsk cathepsin K ISO CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: Pyknodysostosis
PMID:7663522 PMID:8703060 PMID:8938428 PMID:9529353 PMID:10074491 More... RGD:734856 NCBI chr 2:183,058,586...183,069,551
Ensembl chr 2:183,058,569...183,069,550
JBrowse link
G Igf1 insulin-like growth factor 1 ISO associated with Dwarfism; RGD PMID:11474477 RGD:8548826 NCBI chr 7:22,282,895...22,361,972
Ensembl chr 7:22,282,930...22,359,296
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18246
    Developmental Disease 13102
      bone development disease 1904
        osteochondrodysplasia 631
          pycnodysostosis 2
Path 2
Term Annotations click to browse term
  disease 18246
    Developmental Disease 13102
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 11857
        genetic disease 11365
          monogenic disease 8941
            autosomal genetic disease 7989
              autosomal recessive disease 4968
                pycnodysostosis 2
paths to the root