Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the vasculature of the eye (HP:0008047)help
Parent Node:
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Abnormal conjunctiva morphology (HP:0000502)help
Parent Node:
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Red eye (HP:0025337)help
..Starting node
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Conjunctival hyperemia (HP:0030953)help
Term ID: 30953
Name: Conjunctival hyperemia
Synonym: Conjunctival hyperaemia; Conjunctival injection; Conjunctival vascular congestion
Definition: Dilatation of the blood vessels of the conjunctiva leading to a red appearance of the sclera.
Comments:
Reference: HP:0030953
Genes and Diseases:
 
       Child Nodes:
........expandCircumlimbal hyperemia (HP:0025338) help

 Sister Nodes: 
..expandConjunctivitis (HP:0000509) help
..expandDeep episcleral hyperemia (HP:0025340) help
..expandSuperficial episcleral hyperemia (HP:0025339) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0030953HP:0030953Conjunctival hyperemia0NLRP3 CL E G H114548148200Keratitis fugax hereditaria148200C1835697OMIM114216400606416
HP:0030953HP:0030953Conjunctival hyperemia0TNFRSF1A CL E G H7132142680TNF receptor-associated periodic fever syndrome (TRAPS)142680C1275126OMIM110911916191190
HP:0030953HP:0030953Conjunctival hyperemia1NLRP3 CL E G H114548148200Keratitis fugax hereditaria148200C1835697OMIM114216400606416
HP:0030953HP:0030953Conjunctival hyperemia1TNFRSF1A CL E G H7132142680TNF receptor-associated periodic fever syndrome (TRAPS)142680C1275126OMIM110911916191190
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (2) :NLRP3 TNFRSF1A

Diseases (2) :148200 142680
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.