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 incisor (HP:0000676)

Grandparent Node:
Tooth malposition (HP:0000692)

Parent Node:
Misalignment of incisors (HP:0011062)

..Starting node
..Rotated maxillary central incisors (HP:0006330)

Term ID:

6330

Name:

Rotated maxillary central incisors

Synonym:

Rotated upper central incisors; Rotated upper front teeth; Turned upper front teeth; Twisted upper front teeth

Definition:

Comments:

Reference:

HP:0006330

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal spaced incisors (HP:0040159)

Crowded maxillary incisors (HP:0006333)

Forward slanting upper incisors (HP:0025009)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006330	HP:0006330	Rotated maxillary central incisors	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.