PedAM
Pediatric Disease Annotations & Medicines
| Disease | osteogenesis imperfecta |
| Phenotype | C0024899|mastocytosis |
| Sentences | 1 |
| PubMedID- 23079689 | Assessment is guided by the clinical findings, and some patients who apparently have primary osteoporosis are subsequently found to have mild hyperparathyroidism or hyperthyroidism, systemic mastocytosis, the late appearance of osteogenesis imperfecta or osteomalacia. |
Page: 1