Human Phenotype Ontology 
Grandparent Node:
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Abnormal testis morphology (HP:0000035)help
Grandparent Node:
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Gonadal neoplasm (HP:0010785)help
Grandparent Node:
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Neoplasm of the male external genitalia (HP:0100848)help
Parent Node:
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Germinoma (HP:0100620)help
Parent Node:
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Testicular neoplasm (HP:0010788)help
..Starting node
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Testicular seminoma (HP:0100617)help
Term ID: 100617
Name: Testicular seminoma
Synonym:
Definition: The presence of a seminoma, an undifferentiated germ cell tumor of the testis.
Comments:
Reference: HP:0100617
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandLeydig cell neoplasia (HP:0100618) help
..expandSertoli cell neoplasm (HP:0100619) help
..expandTesticular adrenal rest tumor (HP:0025451) help
..expandTesticular gonadoblastoma (HP:0000030) help
..expandTesticular mesothelioma (HP:0100005) help
..expandTesticular teratoma (HP:0100616) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100617HP:0100617Testicular seminoma0DICER1 CL E G H2340517098ORPHA:276399Familial multinodular goiterHP:0040282 - Frequent670
HP:0100617HP:0100617Testicular seminoma0H19-ICR CL E G H105259599OMIM:180860Silver-Russell syndrome.
HP:0100617HP:0100617Testicular seminoma0IGF2 CL E G H34815466OMIM:180860Silver-Russell syndrome.9
HP:0100617HP:0100617Testicular seminoma0KEAP1 CL E G H981723177ORPHA:276399Familial multinodular goiterHP:0040282 - Frequent
HP:0100617HP:0100617Testicular seminoma0STS CL E G H41211425ORPHA:281090Syndromic recessive X-linked ichthyosisHP:0040283 - Occasional19


Genes (5) :DICER1 H19-ICR IGF2 KEAP1 STS

Diseases (3) :ORPHA:276399 OMIM:180860 ORPHA:281090
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.