Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the dentition (HP:0000164)help
Parent Node:
expandAbnormal odontoid tissue morphology (HP:3000050)help
Parent Node:
expandAbnormality of dental structure (HP:0011061)help
..Starting node
..expandAbnormal cementum morphology (HP:0100717)help
Term ID: 100717
Name: Abnormal cementum morphology
Synonym: Abnormality of the cementum
Definition: Any structural anomaly of the cementum, which is the mineralized connective tissue covering the dental root. The cementum allows anchoring of the fibers of the periodontal ligament. Cementum is secreted by cementoblasts, which may be, later on, embedded in the cementum. Cementum can be acellular (along the two third coronal portion of the root) and cellular (in the apical and interradicular part of the root).
Comments:
Reference: HP:0100717
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal dental enamel morphology (HP:0000682) help
..expandAbnormal dental pulp morphology (HP:0006479) help
..expandAbnormal dentin morphology (HP:0010299) help
..expandAbnormality of dental color (HP:0011073) help
..expandCarious teeth (HP:0000670) help
..expandHypoplasia of teeth (HP:0000685) help
..expandTooth abscess (HP:0030757) 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:0100717HP:0100717Abnormal cementum morphology0 CL E G H
HP:0100717HP:0033788Cementum overgrowth1 CL E G H
HP:0100717HP:0033787Cementum hypoplasia1 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.