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)

Parent Node:
Conjunctival follicles (HP:0030947)

..Starting node
..Conjunctival cicatrization (HP:0500039)

Term ID:

500039

Name:

Conjunctival cicatrization

Synonym:

Cicatricial conjunctivitis; Cicatrizating conjunctivitis; Conjunctival cicatricial conjunctivitis

Definition:

An abnormality of the conjuctiva and ocular surface caused by conjunctival inflammation and associated with scarring.

Comments:

Reference:

HP:0500039

Genes and Diseases:

Child Nodes:

........

Dermolipoma of the conjunctiva (HP:0500040)

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:0500039	HP:0500039	Conjunctival cicatrization	0	CL E G H
HP:0500039	HP:0500040	Dermolipoma of the conjunctiva	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.