Meningioma
Symptom Information:
All diseases associated with this symptom:
ACTH-independent macronodular adrenal hyperplasia | (Orphanet:189427) |
BAP1-related tumor predisposition syndrome | (Orphanet:289539) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Cowden syndrome | (Orphanet:201) |
Familial multiple meningioma | (Orphanet:263662) |
Gorlin syndrome | (Orphanet:377) |
HUNTER-MACDONALD SYNDROME | (OMIM:611962) |
LI-FRAUMENI SYNDROME 2 | (OMIM:609265) |
Lhermitte-Duclos disease | (Orphanet:65285) |
Megalencephaly-capillary malformation-polymicrogyria syndrome | (Orphanet:60040) |
Melanoma and neural system tumor syndrome | (Orphanet:252206) |
NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL | (OMIM:162260) |
Neurocutaneous melanocytosis | (Orphanet:2481) |
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion | (Orphanet:363700) |
Neurofibromatosis type 2 | (Orphanet:637) |
Neurofibromatosis type 3 | (Orphanet:93921) |
Proteus syndrome | (Orphanet:744) |
Proteus-like syndrome | (Orphanet:2969) |
SCHWANNOMATOSIS 1 | (OMIM:162091) |
Werner syndrome | (Orphanet:902) |