Human Phenotype Ontology 
Grandparent Node:
expand
All (HP:0000001)help
Parent Node:
expand
Frequency (HP:0040279)help
..Starting node
..expand
Excluded (HP:0040285)help
Term ID: 40285
Name: Excluded
Synonym: Excluded (0%)
Definition: Present in 0% of the cases.
Comments:
Reference: HP:0040285
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFrequent (HP:0040282) help
..expandObligate (HP:0040280) help
..expandOccasional (HP:0040283) help
..expandVery frequent (HP:0040281) help
..expandVery rare (HP:0040284) 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:0040285HP:0040285Excluded0 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.