eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | neurofibromatosis type 1 |
| Symptom | C0018552|hamartoma |
| Sentences | 2 |
| PubMedID- 26398241 | An incidental finding of choroidal ganglioneuronal hamartoma in a patient with neurofibromatosis type 1. |
| PubMedID- 21540621 | Other malformations included: subcortical hamartoma associated with neurofibromatosis type 1, craniofacial dysmorphism secondary to noonan syndrome, congenital occipital plagiocephaly, os odontoideum, craniofacial cleft, juvenile rheumathoid arthritis with platybasia, and osteogenesis imperfecta with bathrocephaly and scoliosis. |
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