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Alveolar soft-part sarcoma
1 OMIM reference -
2 associated genes
39 connected diseases
No signs/symptoms info
Disease Type of connection
Translocation renal cell carcinoma
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Behavioral variant of frontotemporal dementia
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Aneurysm - osteoarthritis syndrome
Familial thoracic aortic aneurysm and aortic dissection
Familial pancreatic carcinoma
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Myhre syndrome
Clear cell renal carcinoma
MITF-related melanoma and renal cell carcinoma predisposition syndrome
Ocular albinism with congenital sensorineural deafness
Papillary renal cell carcinoma
Tietz syndrome
Waardenburg syndrome type 2
Inflammatory myofibroblastic tumor
Coffin-Siris syndrome
Familial multiple meningioma
22q11.2 deletion syndrome
Acute infantile liver failure-multisystemic involvement syndrome
Cone rod dystrophy
Congenital lactic acidosis, Saguenay-Lac-St. Jean type
Familial atrial fibrillation
Intellectual deficit, X-linked, Snyder type
Leber congenital amaurosis
Meckel syndrome
Weaver syndrome
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: D018234
Gene symbol UniProt reference OMIM reference
ASPSCR1 Q9BZE9606236
TFE3 P19532314310
No signs/symptoms info available.