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cranioosteoarthropathy
Genetics:
- associated with defects in HPGD
Clinical manifestations:
- infantile onset
- swelling of the joints
- digital clubbing
- hyperhidrosis
- delayed closure of the fontanels
- periostosis
- variable patent ductus arteriosus
- pachydermia is not a prominent feature
General
osteoarthropathy
genetic disease of bone/skeletal system
Database Correlations
OMIM 259100
References
OMIM :accession 259100