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:
Strabismus (HP:0000486)

Parent Node:
Exotropia (HP:0000577)

Parent Node:
obsolete Congenital strabismus (HP:0000487)

..Starting node
..obsolete Congenital exotropia (HP:0008033)

Term ID:

8033

Name:

obsolete Congenital exotropia

Synonym:

Definition:

Comments:

Reference:

HP:0008033

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008033	HP:0008033	obsolete Congenital exotropia	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.