eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | neurofibromatosis type 1 |
| Comorbidity | C0085113|neurofibromatosis |
| Sentences | 2 |
| PubMedID- 23460398 | Germline heterozygous alterations of the tumor-suppressor gene neurofibromatosis-1 (nf1) lead to neurofibromatosis type 1, a genetic disorder characterized by a higher risk to develop juvenile myelomonocytic leukemia and/or acute myeloid leukemia (aml). |
| PubMedID- 23417386 | Spinal neurofibromatosis associated with classical neurofibromatosis type 1: genetic characterisation of an atypical case. |
Page: 1