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
..Notched primary central incisor (HP:0012413)

Term ID:

12413

Name:

Notched primary central incisor

Synonym:

Notched front baby tooth; Notched front deciduous tooth; Notched front primary tooth; Syphilitic primary incisor

Definition:

The presence of a V-shaped indentation (notch) in the primary central incisor.

Comments:

Reference:

HP:0012413

Genes and Diseases:

Child Nodes:

Sister Nodes:

Conical incisor (HP:0011065)

Dens in dente (HP:0011088)

Discolored lateral incisors (HP:0006290)

Incisor macrodontia (HP:0011081)

Maxillary lateral incisor microdontia (HP:0001593)

Screwdriver-shaped incisors (HP:0006346)

Shovel-shaped maxillary central incisors (HP:0006358)

Talon cusp (HP:0011087)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012413	HP:0012413	Notched primary central incisor	0	DPH2 CL E G H	1802	3004	OMIM:620062

Genes (1) :DPH2

Diseases (1) :OMIM:620062

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