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 structure (HP:0011061)

Parent Node:
Abnormality of dental color (HP:0011073)

..Starting node
..White streaks/specks on enamel. (HP:0025123)

Term ID:

25123

Name:

White streaks/specks on enamel.

Synonym:

Definition:

Areas of white discoloration visible on the surface of the teeth (enamel) in the form of streaks or specks.

Comments:

Reference:

HP:0025123

Genes and Diseases:

Child Nodes:

Sister Nodes:

Erythrodontia (HP:0030756)

Grayish enamel (HP:0000683)

Green teeth (HP:0011075)

Yellow-brown discoloration of the teeth (HP:0006286)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025123	HP:0025123	White streaks/specks on enamel.	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.