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Osteonecrosis of genetic origin
rareAn instance of osteonecrosis that is caused by a modification of the individual's genome.
- Identifiers
- MONDO:0018383 Orphanet:399380
- Part of
- Hereditary diseaseOsteonecrosis
- Also known as
- bone necrosis of genetic origin · genetic osteonecrosis
Subtypes
Disease Rare Not rare Subtypes
- Familial avascular necrosis of femoral head MONDO:0012126 2
- Gaucher disease type I MONDO:0009265 GBA1
- Legg-Calve-Perthes disease MONDO:0007885 COL2A1
- Scheuermann disease MONDO:0008410
- Thiemann disease, familial form MONDO:0008142
- Dihydropyrimidine dehydrogenase deficiency MONDO:0010130 DPYD
- Epiphysiolysis of the hip MONDO:0018382
- Hereditary antithrombin deficiency MONDO:0013144 SERPINC1
- Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency MONDO:0013143 HRG
- Osteochondritis dissecans MONDO:0017178
- Pseudohypoparathyroidism type 1C MONDO:0012911 GNAS
- Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans MONDO:0100462
Projects
Including projects on subtypes.
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