ODCs

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Testicular seminomatous germ cell tumor

1 OMIM reference -
3 associated genes
30 connected diseases
No signs/symptoms info

Disease	Type of connection
Testicular non seminomatous germ cell tumor
Familial progressive hyper- and hypopigmentation
Familial progressive hyperpigmentation
Kallmann syndrome
Normosmic congenital hypogonadotropic hypogonadism
Primary ciliary dyskinesia
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): - Dysgerminoma of the testis - Dysgerminomatous germ cell tumor of the testis - Seminoma of the testis - Seminomatous germ cell tumor of the testis - Testicular dysgerminoma - Testicular dysgerminomatous germ cell tumor - Testicular seminoma

Classification (Orphanet): - Rare oncologic disease - Rare urogenital disease		Classification (ICD10): - Neoplasms -

Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: any age Type of inheritance: sporadic		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.