Human Phenotype Ontology 
Parent Node:
expand
All (HP:0000001)help
..Starting node
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Frequency (HP:0040279)help
Term ID: 40279
Name: Frequency
Synonym:
Definition: Class to represent frequency of phenotypic abnormalities within a patient cohort.
Comments:
Reference: HP:0040279
Genes and Diseases:
 
       Child Nodes:
........expandObligate (HP:0040280) help
........expandVery frequent (HP:0040281) help
........expandFrequent (HP:0040282) help
........expandOccasional (HP:0040283) help
........expandVery rare (HP:0040284) help
........expandExcluded (HP:0040285) help

 Sister Nodes: 
..expandClinical course (HP:0031797) help
..expandClinical modifier (HP:0012823) help
..expandMode of inheritance (HP:0000005) help
..expandPhenotypic abnormality (HP:0000118) 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:0040279HP:0040279Frequency0 CL E G H
HP:0040279HP:0040285Excluded1 CL E G H
HP:0040279HP:0040284Very rare1 CL E G H
HP:0040279HP:0040283Occasional1 CL E G H
HP:0040279HP:0040282Frequent1 CL E G H
HP:0040279HP:0040281Very frequent1 CL E G H
HP:0040279HP:0040280Obligate1 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.