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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Gonadoblastoma (HP:0000150)help
Parent Node:
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Testicular neoplasm (HP:0010788)help
..Starting node
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Testicular gonadoblastoma (HP:0000030)help
Term ID: 30
Name: Testicular gonadoblastoma
Synonym: Gonadoblastoma, male
Definition: The presence of a gonadoblastoma of the testis.
Comments:
Reference: HP:0000030
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 mesothelioma (HP:0100005) help
..expandTesticular seminoma (HP:0100617) 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:0000030HP:0000030Testicular gonadoblastoma0DHX37 CL E G H5764717210ORPHA:25151046,XY partial gonadal dysgenesisHP:0040283 - Occasional2
HP:0000030HP:0000030Testicular gonadoblastoma0DMRT3 CL E G H5852413909ORPHA:25151046,XY partial gonadal dysgenesisHP:0040283 - Occasional1
HP:0000030HP:0000030Testicular gonadoblastoma0GATA4 CL E G H26264173ORPHA:25151046,XY partial gonadal dysgenesisHP:0040283 - Occasional87
HP:0000030HP:0000030Testicular gonadoblastoma0MAP3K1 CL E G H42146848ORPHA:25151046,XY partial gonadal dysgenesisHP:0040283 - Occasional13
HP:0000030HP:0000030Testicular gonadoblastoma0NR0B1 CL E G H1907960ORPHA:25151046,XY partial gonadal dysgenesisHP:0040283 - Occasional48
HP:0000030HP:0000030Testicular gonadoblastoma0NR5A1 CL E G H25167983ORPHA:25151046,XY partial gonadal dysgenesisHP:0040283 - Occasional38
HP:0000030HP:0000030Testicular gonadoblastoma0SOX9 CL E G H666211204ORPHA:25151046,XY partial gonadal dysgenesisHP:0040283 - Occasional109
HP:0000030HP:0000030Testicular gonadoblastoma0SRY CL E G H673611311ORPHA:25151046,XY partial gonadal dysgenesisHP:0040283 - Occasional23
HP:0000030HP:0000030Testicular gonadoblastoma0VAMP7 CL E G H684511486ORPHA:25151046,XY partial gonadal dysgenesisHP:0040283 - Occasional2
HP:0000030HP:0000030Testicular gonadoblastoma0WT1 CL E G H749012796ORPHA:25151046,XY partial gonadal dysgenesisHP:0040283 - Occasional177
HP:0000030HP:0000030Testicular gonadoblastoma0WWOX CL E G H5174112799ORPHA:25151046,XY partial gonadal dysgenesisHP:0040283 - Occasional149
HP:0000030HP:0000030Testicular gonadoblastoma0ZFPM2 CL E G H2341416700ORPHA:25151046,XY partial gonadal dysgenesisHP:0040283 - Occasional31


Genes (12) :DHX37 DMRT3 GATA4 MAP3K1 NR0B1 NR5A1 SOX9 SRY VAMP7 WT1 WWOX ZFPM2

Diseases (1) :ORPHA:251510
 

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