Human Phenotype Ontology 
Grandparent Node:
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Autosomal dominant inheritance (HP:0000006)help
Parent Node:
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Sex-limited expression (HP:0001470)help
..Starting node
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Male-limited expression (HP:0001475)help
Term ID: 1475
Name: Male-limited expression
Synonym:
Definition: Used to refer to a monogenic trait linked to an autosomal locus in which the phenotypic effects of allelic differences are expressed only in the male sex.
Comments:
Reference: HP:0001475
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001475HP:0001475Male-limited expression0 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 December 15 2022 release.