Loss of heterozygosity for 17p sequences in 45% of medulloblastomas

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Loss of heterozygosity for 17p sequences in 45% of medulloblastomas" [OMIM:Loss of heterozygosity for 17p sequences in 45% of medulloblastomas]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Classic medulloblastoma (Orphanet:251867)
Desmoplastic/nodular medulloblastoma (Orphanet:251863)
Medulloblastoma (Orphanet:616)
Medulloblastoma with extensive nodularity (Orphanet:251858)