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Testicular non seminomatous germ cell tumor
1 OMIM reference -
2 associated genes
29 connected diseases
No signs/symptoms info
Disease Type of connection
Testicular seminomatous germ cell tumor
Familial progressive hyper- and hypopigmentation
Familial progressive hyperpigmentation
Kallmann syndrome
Normosmic congenital hypogonadotropic hypogonadism
Acute myeloblastic leukemia with maturation
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Aleukemic mast cell leukemia
Bullous diffuse cutaneous mastocytosis
Classic mast cell leukemia
Cutaneous mastocytoma
Gastrointestinal stromal tumor
Isolated bone marrow mastocytosis
Lymphoadenopathic mastocytosis with eosinophilia
Nodular urticaria pigmentosa
Piebaldism
Plaque-form urticaria pigmentosa
Pseudoxanthomatous diffuse cutaneous mastocytosis
Smouldering systemic mastocytosis
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
Telangiectasia macularis eruptiva perstans
Typical urticaria pigmentosa
Juvenile myelomonocytic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
LEOPARD syndrome
Noonan syndrome
Pilocytic astrocytoma
Primary familial polycythemia
Synonym(s):
- Non-seminomatous germ cell tumor of the testis
- Testicular non-dysgerminomatous germ cell tumor
- non-dysgerminomatous germ cell tumor of the testis
Classification (Orphanet):
- Rare oncologic disease
- Rare urogenital disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
KITLG P21583184745
SPRY4 Q9C004607984
No signs/symptoms info available.