Human Phenotype Ontology 
Grandparent Node:
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Phenotypic variability (HP:0003812)help
Parent Node:
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Incomplete penetrance (HP:0003829)help
..Starting node
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Age-dependent penetrance (HP:0003831)help
Term ID: 3831
Name: Age-dependent penetrance
Synonym: Age dependent penetrance
Definition: A situation in which phenotypic abnormalities become evident with age.
Comments:
Reference: HP:0003831
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0003831HP:0003831Age-dependent penetrance0DCHS1 CL E G H8642607829Mitral valve prolapse 2607829C1843003OMIM150213681603057
HP:0003831HP:0003831Age-dependent penetrance0DCHS1 CL E G H8642607829Mitral valve prolapse 2607829C1843003OMIM134713681603057
HP:0003831HP:0003831Age-dependent penetrance0GUCY2D CL E G H3000601777Cone-rod dystrophy 6601777C1866293OMIM15934689600179
HP:0003831HP:0003831Age-dependent penetrance0GUCY2D CL E G H3000601777Cone-rod dystrophy 6601777C1866293OMIM17314689600179
HP:0003831HP:0003831Age-dependent penetrance0TENM4 CL E G H26011616736Tremor, hereditary essential, 5616736C4225223OMIM18629945610084
HP:0003831HP:0003831Age-dependent penetrance0TENM4 CL E G H26011616736Tremor, hereditary essential, 5616736C4225223OMIM19329945610084
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (3) :DCHS1 GUCY2D TENM4

Diseases (3) :607829 601777 616736
 

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