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Accession:DOID:0080038 term browser browse the term
Definition:Rare autosomal recessive syndrome characterized by delayed closing of CRANIAL SUTURES, short stature, ACRO-OSTEOLYSIS of distal phalanges, dental and MAXILLOFACIAL ABNORMALITIES and an increase in bone density that results in frequent BONE FRACTURES. It is associated with BONE RESORPTION defect due to mutations in the lysosomal cysteine protease CATHEPSIN K.
Synonyms:exact_synonym: PKND;   PYCD;   pycnodysostoses;   pyknodysostoses;   pyknodysostosis
 primary_id: MESH:D058631
 alt_id: OMIM:265800;   RDO:0007845
 xref: GARD:4611;   ORDO:763
For additional species annotation, visit the Alliance of Genome Resources.

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pycnodysostosis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ctsk cathepsin K JBrowse link 2 196,655,469 196,666,447 RGD:734856
G Igf1 insulin-like growth factor 1 JBrowse link 7 28,412,123 28,491,815 RGD:8548826

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15625
    Developmental Diseases 8759
      bone development disease 996
        osteochondrodysplasia 410
          pycnodysostosis 2
Path 2
Term Annotations click to browse term
  disease 15625
    Developmental Diseases 8759
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7543
        genetic disease 7038
          monogenic disease 4656
            autosomal genetic disease 3617
              autosomal recessive disease 2056
                pycnodysostosis 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.