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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Testicular neoplasm (HP:0010788)help
..Starting node
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Sertoli cell neoplasm (HP:0100619)help
Term ID: 100619
Name: Sertoli cell neoplasm
Synonym: Sertoli cell neoplasia
Definition: The presence of a neoplasm of the testis with origin in a Sertoli cell.
Comments:
Reference: HP:0100619
Genes and Diseases:
 
       Child Nodes:
........expandPrecocious puberty with Sertoli cell tumor (HP:0008204) help

 Sister Nodes: 
..expandLeydig cell neoplasia (HP:0100618) help
..expandTesticular adrenal rest tumor (HP:0025451) help
..expandTesticular gonadoblastoma (HP:0000030) 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:0100619HP:0100619Sertoli cell neoplasm0DICER1 CL E G H2340517098ORPHA:276399Familial multinodular goiterHP:0040282 - Frequent670
HP:0100619HP:0100619Sertoli cell neoplasm0KEAP1 CL E G H981723177ORPHA:276399Familial multinodular goiterHP:0040282 - Frequent
HP:0100619HP:0100619Sertoli cell neoplasm0PDE11A CL E G H509408773ORPHA:1359Carney complexHP:0040284 - Very rare13
HP:0100619HP:0100619Sertoli cell neoplasm0PRKAR1A CL E G H55739388ORPHA:1359Carney complexHP:0040284 - Very rare134
HP:0100619HP:0100619Sertoli cell neoplasm0STK11 CL E G H679411389OMIM:175200Peutz-Jeghers syndrome740
HP:0100619HP:0008204Precocious puberty with Sertoli cell tumor1STK11 CL E G H679411389OMIM:175200Peutz-Jeghers syndrome.740


Genes (5) :DICER1 KEAP1 PDE11A PRKAR1A STK11

Diseases (3) :ORPHA:276399 ORPHA:1359 OMIM:175200
 

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