An instance of osteonecrosis that is caused by a modification of the individual's genome.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| 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 |
Rare disease
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