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Synovial sarcoma
1 OMIM reference -
3 associated genes
17 connected diseases
No signs/symptoms info
Disease Type of connection
Coffin-Siris syndrome
Familial rhabdoid tumor
Intellectual deficit - sparse hair - brachydactyly
17q11 microdeletion syndrome
Extraskeletal Ewing sarcoma
Weaver syndrome
Atypical teratoid tumor
Familial multiple meningioma
Neurofibromatosis type 3
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Precursor T-cell acute lymphoblastic leukemia
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
Pituitary stalk interruption syndrome
Pseudohypoaldosteronism type 2E
Short stature - pituitary and cerebellar defects - small sella turcica
Synonym(s):
- Synovialosarcoma
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SS18 Q15532600192
SSX1 Q16384312820
SSX2 Q16385300192
No signs/symptoms info available.