Optic glioma
Symptom Information:
All diseases associated with this symptom:
17q11 microdeletion syndrome | (Orphanet:97685) |
17q11.2 microduplication syndrome | (Orphanet:139474) |
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion | (Orphanet:363700) |
TUBEROUS SCLEROSIS 1 | (OMIM:191100) |
TUBEROUS SCLEROSIS 2 | (OMIM:613254) |
Tuberous sclerosis | (Orphanet:805) |
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME | (OMIM:601321) |