Human Phenotype Ontology 
..Starting node
..expandFemale-limited expression (HP:0034344)help
Term ID: 34344
Name: Female-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 female sex.
Comments:
Reference: HP:0034344
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:0034344HP:0034344Female-limited expression0POF1B CL E G H7998313711OMIM:300604Premature ovarian failure 2B31


Genes (1) :POF1B

Diseases (1) :OMIM:300604
 

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