Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the vasculature (HP:0002597)help
Grandparent Node:
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obsolete Abnormal globe morphology (HP:0012374)help
Parent Node:
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Abnormal conjunctiva morphology (HP:0000502)help
Parent Node:
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Abnormality of the vasculature of the eye (HP:0008047)help
..Starting node
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Abnormal morphology of the conjunctival vasculature (HP:0008054)help
Term ID: 8054
Name: Abnormal morphology of the conjunctival vasculature
Synonym: Abnormal morphology of the conjunctiva vasculature; Abnormal vasculature of the conjunctiva morphology; Abnormality of the vasculature of the conjunctiva
Definition: Any abnormality of the blood vessels of the conjunctiva.
Comments:
Reference: HP:0008054
Genes and Diseases:
 
       Child Nodes:
........expandTortuosity of conjunctival vessels (HP:0000503) help
........expandConjunctival telangiectasia (HP:0000524) help
........expandSaccular conjunctival dilatations (HP:0007721) help

 Sister Nodes: 
..expandAbnormal iris vasculature (HP:0007905) help
..expandAbnormal retinal vascular morphology (HP:0008046) help
..expandRed eye (HP:0025337) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008054HP:0008054Abnormal morphology of the conjunctival vasculature0 CL E G H
HP:0008054HP:0008054Abnormal morphology of the conjunctival vasculature1 CL E G H


Genes (24) :ACVRL1 ANO10 ATM CTSA DDB2 ENG ERCC2 ERCC3 ERCC4 ERCC5 FUCA1 GDF2 GLA GNAQ MANBA MASP1 PCNA PEX6 RNF168 SETX SLC52A2 SMAD4 XPA XPC

Diseases (16) :774 600376 284289 208900 256540 910 187300 230000 324 3205 248510 257920 615919 95433 420741 606002
 

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