hypertrophic osteoarthropathy, primary, autosomal recessive, 1
ORPHA: 1525
Overview
human disease
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with hypertrophic osteoarthropathy, primary, autosomal recessive, 1, sourced from HPO and Orphanet clinical annotations.
Large fontanellesAbnormal skull morphologyEczematoid dermatitisMottled pigmentationArthritisJoint swellingJoint stiffnessOsteoarthritisAbnormality of the kneeArthralgiaAbnormal tibia morphologyAbnormal cortical bone morphologyDeviation of fingerClubbing of toes
Classification & Codes
Orphanet Code
ORPHA:1525hypertrophic osteoarthropathy, primary, autosomal recessive, 1
| Orphanet | ORPHA:1525 |
| Treatments | 0 drug(s) |
| Symptoms on record | 14 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO