Neuroblastoma
Symptom Information:
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Beckwith-Wiedemann syndrome | (Orphanet:116) |
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Constitutional mismatch repair deficiency syndrome | (Orphanet:252202) |
Dubowitz syndrome | (Orphanet:235) |
FANCONI ANEMIA, COMPLEMENTATION GROUP N | (OMIM:610832) |
Familial platelet syndrome with predisposition to acute myelogenous leukemia | (Orphanet:71290) |
Haddad syndrome | (Orphanet:99803) |
Hereditary pheochromocytoma-paraganglioma | (Orphanet:29072) |
Neuroblastoma | (Orphanet:635) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Ondine syndrome | (Orphanet:661) |
PARAGANGLIOMAS 4 | (OMIM:115310) |
PLATELET DISORDER, UNDEFINED | (OMIM:173420) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |