Human Phenotype Ontology

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Hello! Guest! Please Login or Register! Clinician Mode

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 structure (HP:0011061)

Parent Node:
Abnormal dental pulp morphology (HP:0006479)

..Starting node
..Pulp obliteration (HP:0006350)

Term ID:

6350

Name:

Pulp obliteration

Synonym:

Crescent/chevron-shaped pulp chambers; Narrowing of pulp chamber of tooth; Obliteration of the pulp chamber; Pulp canal obliteration; Reduced size of pulp chamber of tooth; Small pulp chamber of tooth

Definition:

Mineralized substance filling the entire dental pulp space.

Comments:

Reference:

HP:0006350

Genes and Diseases:

Child Nodes:

Sister Nodes:

Dagger-shaped pulp calcifications (HP:0006302)

Pulp calcification (HP:0003771)

Taurodontia (HP:0000679)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006350	HP:0006350	Pulp obliteration	0	SMOC2 CL E G H	64094	20323	OMIM:125400	Dentin dysplasia, type I, with microdontia and misshapen teeth	.	4

Genes (1) :SMOC2

Diseases (1) :OMIM:125400

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

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