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:
Abnormal conjunctiva morphology (HP:0000502)

Grandparent Node:
Inflammatory abnormality of the eye (HP:0100533)

Grandparent Node:
Red eye (HP:0025337)

Parent Node:
Allergy (HP:0012393)

Parent Node:
Conjunctivitis (HP:0000509)

..Starting node
..Allergic conjunctivitis (HP:0007879)

Term ID:

7879

Name:

Allergic conjunctivitis

Synonym:

Definition:

Allergic Conjunctivitis is an allergic inflammation of the conjunctiva.

Comments:

Reference:

HP:0007879

Genes and Diseases:

Child Nodes:

Sister Nodes:

Chronic irritative conjunctivitis (HP:0007717)

Keratoconjunctivitis (HP:0001096)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007879	HP:0007879	Allergic conjunctivitis	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.