Human Phenotype Ontology 
Grandparent Node:
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Abnormal oral cavity morphology (HP:0000163)help
Parent Node:
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Abnormality of the dentition (HP:0000164)help
..Starting node
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Fragile teeth (HP:0025124)help
Term ID: 25124
Name: Fragile teeth
Synonym: Enamel with tendency to chip; Spontaneous tooth fracture
Definition: A tendency of teeth to fracture as manifested by a history of repeated fracture of the dental enamel without adequate trauma.
Comments:
Reference: HP:0025124
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal number of teeth (HP:0006483) help
..expandAbnormal periodontium morphology (HP:0410026) help
..expandAbnormality of canine (HP:0011078) help
..expandAbnormality of dental eruption (HP:0006292) help
..expandAbnormality of dental morphology (HP:0006482) help
..expandAbnormality of dental structure (HP:0011061) help
..expandAbnormality of molar (HP:0011077) help
..expandAbnormality of premolar (HP:0011076) help
..expandAbnormality of primary teeth (HP:0006481) help
..expandAbnormality of the incisor (HP:0000676) help
..expandBuried teeth encased in mucopolysaccharide (HP:0006326) help
..expandIrregular dentition (HP:0040079) help
..expandOdontogenic neoplasm (HP:0100612) help
..expandPeriapical bone loss (HP:0000700) help
..expandPeriodontitis (HP:0000704) help
..expandPremature loss of teeth (HP:0006480) help
..expandTooth malposition (HP:0000692) 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:0025124HP:0025124Fragile teeth0TNFRSF11A CL E G H879211908OMIM:174810Familial expansile osteolysis.72


Genes (1) :TNFRSF11A

Diseases (1) :OMIM:174810
 

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