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 the dentition (HP:0000164)

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

Parent Node:
Abnormality of premolar (HP:0011076)

..Starting node
..Abnormal premolar morphology (HP:0011080)

Term ID:

11080

Name:

Abnormal premolar morphology

Synonym:

Abnormality of bicuspid morphology; Abnormality of premolar morphology; Abnormality of shape of bicuspid; Abnormality of shape of premolar

Definition:

An abnormality of morphology of premolar tooth.

Comments:

Reference:

HP:0011080

Genes and Diseases:

Child Nodes:

........

Malformation of mandibular premolar (HP:0006338)

........

Molarization of premolar (HP:0011093)

Sister Nodes:

Agenesis of premolar (HP:0011051)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011080	HP:0011080	Abnormal premolar morphology	0	CL E G H
HP:0011080	HP:0011093	Molarization of premolar	1	CL E G H
HP:0011080	HP:0006338	Malformation of mandibular premolar	1	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.