Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 cornea morphology (HP:0000481)

Parent Node:
Abnormal corneal endothelium morphology (HP:0011488)

..Starting node
..Corneal keratic precipitates (HP:0025341)

Term ID:

25341

Name:

Corneal keratic precipitates

Synonym:

Definition:

An inflammatory cellular deposit deposited on the corneal endothelium and visible as spots on the cornea.

Comments:

Reference:

HP:0025341

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal Descemet membrane morphology (HP:0011490)

Abnormal migration of corneal endothelium (HP:0011489)

Reduced number of corneal endothelial cells (HP:0011491)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025341	HP:0025341	Corneal keratic precipitates	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.