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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Abnormality of the Leydig cells (HP:0010789)help
Parent Node:
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Testicular neoplasm (HP:0010788)help
..Starting node
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Leydig cell neoplasia (HP:0100618)help
Term ID: 100618
Name: Leydig cell neoplasia
Synonym:
Definition: The presence of a neoplasm of the testis with origin in a Leydig cell.
Comments:
Reference: HP:0100618
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandSertoli cell neoplasm (HP:0100619) 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 entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100618HP:0100618Leydig cell neoplasia0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.