Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormality of dental morphology (HP:0006482)

Grandparent Node:
Abnormality of the incisor (HP:0000676)

Parent Node:
Abnormal incisor morphology (HP:0011063)

..Starting node
..Dens in dente (HP:0011088)

Term ID:

11088

Name:

Dens in dente

Synonym:

Dens invaginatus; Tooth within a tooth

Definition:

An abnormality of the incisor characterized by invagination of the enamel, giving a radiographic appearance that suggests a tooth within a tooth.

Comments:

Reference:

HP:0011088

Genes and Diseases:

Child Nodes:

Sister Nodes:

Conical incisor (HP:0011065)

Discolored lateral incisors (HP:0006290)

Incisor macrodontia (HP:0011081)

Maxillary lateral incisor microdontia (HP:0001593)

Notched primary central incisor (HP:0012413)

Screwdriver-shaped incisors (HP:0006346)

Shovel-shaped maxillary central incisors (HP:0006358)

Talon cusp (HP:0011087)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011088	HP:0011088	Dens in dente	0	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.