Human Phenotype Ontology 
Grandparent Node:
expandAbnormal dental enamel morphology (HP:0000682)help
Grandparent Node:
expandHypoplasia of teeth (HP:0000685)help
Parent Node:
expandEnamel hypoplasia (HP:0006297)help
..Starting node
..expandGeneralized hypoplasia of dental enamel (HP:0006282)help
Term ID: 6282
Name: Generalized hypoplasia of dental enamel
Synonym: Generalised dysplasia of tooth enamel; Generalised hypoplasia of dental enamel; Generalised hypoplasia of tooth enamel; Generalized dysplasia of tooth enamel; Generalized hypoplasia of tooth enamel
Definition: A generalized form of developmental hypoplasia of the dental enamel.
Comments:
Reference: HP:0006282
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandLocalized hypoplasia of dental enamel (HP:0011074) 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:0006282HP:0006282Generalized hypoplasia of dental enamel0 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.