Human Phenotype Ontology 
Grandparent Node:
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Abnormal anterior eye segment morphology (HP:0004328)help
Parent Node:
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Abnormal cornea morphology (HP:0000481)help
..Starting node
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Corneal neovascularization (HP:0011496)help
Term ID: 11496
Name: Corneal neovascularization
Synonym: Corneal neovascularisation; Corneal vascularization; Limbal neovascularization; New blood vessel formation in cornea
Definition: Ingrowth of new blood vessels into the cornea.
Comments:
Reference: HP:0011496
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal corneal endothelium morphology (HP:0011488) help
..expandAbnormal corneal epithelium morphology (HP:0011495) help
..expandAbnormality of corneal shape (HP:0040004) help
..expandAbnormality of corneal size (HP:0001120) help
..expandAbnormality of corneal stroma (HP:0011492) help
..expandAbnormality of corneal thickness (HP:0011486) help
..expandAbnormality of the corneal limbus (HP:0025348) help
..expandAbnormality of the curvature of the cornea (HP:0100691) help
..expandAbnormality of the line of Schwalbe (HP:0008048) help
..expandCornea verticillata (HP:0500008) help
..expandCorneal degeneration (HP:0007705) help
..expandCorneal dystrophy (HP:0001131) help
..expandCorneal opacity (HP:0007957) help
..expandCorneal perforation (HP:0100583) help
..expandDecreased corneal reflex (HP:0008000) help
..expandDecreased corneal sensation (HP:0012155) help
..expandLimbal dermoid (HP:0001140) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0011496HP:0011496Corneal neovascularization0ARVCF CL E G H421567ORPHA12477728602269
HP:0011496HP:0011496Corneal neovascularization0COMT CL E G H1312567ORPHA1155552228116790
HP:0011496HP:0011496Corneal neovascularization0CYP1B1 CL E G H1545617315Anterior segment dysgenesis 6617315C4310623OMIM12432162597601771
HP:0011496HP:0011496Corneal neovascularization0FOXE3 CL E G H230188632ORPHA131863808601094
HP:0011496HP:0011496Corneal neovascularization0GJB2 CL E G H2706477ORPHA14103854284121011
HP:0011496HP:0011496Corneal neovascularization0GJB6 CL E G H10804477ORPHA1341574288604418
HP:0011496HP:0011496Corneal neovascularization0GP1BB CL E G H2812567ORPHA1534044440138720
HP:0011496HP:0011496Corneal neovascularization0HIRA CL E G H7290567ORPHA153994916600237
HP:0011496HP:0011496Corneal neovascularization0JMJD1C CL E G H221037567ORPHA12950912313604503
HP:0011496HP:0011496Corneal neovascularization0NLRP1 CL E G H22861617388Autoinflammation with arthritis and dyskeratosis617388C4479278OMIM11813414374606636
HP:0011496HP:0011496Corneal neovascularization0NLRP1 CL E G H22861615225Palmoplantar carcinoma, multiple self-healing615225C3808876OMIM11813414374606636
HP:0011496HP:0011496Corneal neovascularization0PITX3 CL E G H530988632ORPHA115299006602669
HP:0011496HP:0011496Corneal neovascularization0RREB1 CL E G H6239567ORPHA11217110449602209
HP:0011496HP:0011496Corneal neovascularization0SEC24C CL E G H9632567ORPHA12410705607185
HP:0011496HP:0011496Corneal neovascularization0TBX1 CL E G H6899567ORPHA18255311592602054
HP:0011496HP:0011496Corneal neovascularization0UFD1 CL E G H7353567ORPHA1436812520601754
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011496HP:0011496Corneal neovascularization0COL4A1 CL E G H1282607595Brain small vessel disease with hemorrhage607595C1843512OMIM01144982202120130
HP:0011496HP:0011496Corneal neovascularization0ERCC2 CL E G H2068278730Xeroderma pigmentosum, group D278730C0268138OMIM01082273434126340


Genes (17) :ARVCF COL4A1 COMT CYP1B1 ERCC2 FOXE3 GJB2 GJB6 GP1BB HIRA JMJD1C NLRP1 PITX3 RREB1 SEC24C TBX1 UFD1

Diseases (8) :567 607595 617315 278730 88632 477 617388 615225
 

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