Human Phenotype Ontology 
Grandparent Node:
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Abnormal eye physiology (HP:0012373)help
Parent Node:
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Abnormal intraocular pressure (HP:0012632)help
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Asymmetry of intraocular pressure (HP:0012633)help
Term ID: 12633
Name: Asymmetry of intraocular pressure
Synonym:
Definition: A difference in the amount of intraocular pressure in the right and left eye.
Comments:
Reference: HP:0012633
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandOcular hypertension (HP:0007906) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012633HP:0012633Asymmetry of intraocular pressure0ADAMTS17 CL E G H17069117109OMIM:613195Weill-Marchesani syndrome 4214
HP:0012633HP:0012633Asymmetry of intraocular pressure0ASB10 CL E G H13637117185OMIM:603383GLAUCOMA 1, OPEN ANGLE, F; GLC1F54
HP:0012633HP:0012633Asymmetry of intraocular pressure0ASPH CL E G H444757OMIM:601552Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs4
HP:0012633HP:0012633Asymmetry of intraocular pressure0BAP1 CL E G H8314950ORPHA:39044Uveal melanoma184
HP:0012633HP:0012633Asymmetry of intraocular pressure0C1QTNF5 CL E G H11490214344ORPHA:67042Late-onset retinal degeneration20
HP:0012633HP:0012633Asymmetry of intraocular pressure0CHST14 CL E G H11318924464ORPHA:2953Musculocontractural Ehlers-Danlos syndrome27
HP:0012633HP:0012633Asymmetry of intraocular pressure0COL18A1 CL E G H807812195OMIM:618880GLAUCOMA, PRIMARY CLOSED-ANGLE; GLCC177
HP:0012633HP:0012633Asymmetry of intraocular pressure0COL2A1 CL E G H12802200ORPHA:93315Spondylometaphyseal dysplasia, 'corner fracture' type284
HP:0012633HP:0012633Asymmetry of intraocular pressure0COL8A2 CL E G H12962216ORPHA:98973Posterior polymorphous corneal dystrophy3
HP:0012633HP:0012633Asymmetry of intraocular pressure0CYP1B1 CL E G H15452597OMIM:231300Glaucoma 3, primary congenital, A101
HP:0012633HP:0012633Asymmetry of intraocular pressure0CYP1B1 CL E G H15452597ORPHA:98977Juvenile glaucoma101
HP:0012633HP:0012633Asymmetry of intraocular pressure0CYSLTR2 CL E G H5710518274ORPHA:39044Uveal melanoma1
HP:0012633HP:0012633Asymmetry of intraocular pressure0DSE CL E G H2994021144ORPHA:2953Musculocontractural Ehlers-Danlos syndrome13
HP:0012633HP:0012633Asymmetry of intraocular pressure0EFEMP1 CL E G H22023218ORPHA:98977Juvenile glaucoma54
HP:0012633HP:0012633Asymmetry of intraocular pressure0FN1 CL E G H23353778ORPHA:93315Spondylometaphyseal dysplasia, 'corner fracture' type9
HP:0012633HP:0012633Asymmetry of intraocular pressure0FOXE3 CL E G H23013808OMIM:610256Anterior segment dysgenesis 223
HP:0012633HP:0012633Asymmetry of intraocular pressure0GNA11 CL E G H27674379ORPHA:39044Uveal melanoma16
HP:0012633HP:0012633Asymmetry of intraocular pressure0GNAQ CL E G H27764390ORPHA:39044Uveal melanoma7
HP:0012633HP:0012633Asymmetry of intraocular pressure0GRHL2 CL E G H799772799ORPHA:98973Posterior polymorphous corneal dystrophy33
HP:0012633HP:0012633Asymmetry of intraocular pressure0HLA-A CL E G H31054931ORPHA:179Birdshot chorioretinopathy4
HP:0012633HP:0012633Asymmetry of intraocular pressure0HMX1 CL E G H31665017OMIM:612109Oculoauricular syndrome2
HP:0012633HP:0012633Asymmetry of intraocular pressure0LMX1B CL E G H40106654ORPHA:2614Nail-patella syndrome165
HP:0012633HP:0012633Asymmetry of intraocular pressure0LOXL1 CL E G H40166665OMIM:177650Exfoliation syndrome.3
HP:0012633HP:0012633Asymmetry of intraocular pressure0LTBP2 CL E G H40536715OMIM:614819Weill-Marchesani syndrome 3123
HP:0012633HP:0012633Asymmetry of intraocular pressure0MYOC CL E G H46537610ORPHA:98977Juvenile glaucoma47
HP:0012633HP:0012633Asymmetry of intraocular pressure0NFIA CL E G H47747784ORPHA:4019861p31p32 microdeletion syndrome12
HP:0012633HP:0012633Asymmetry of intraocular pressure0OVOL2 CL E G H5849515804ORPHA:98973Posterior polymorphous corneal dystrophy4
HP:0012633HP:0012633Asymmetry of intraocular pressure0PITX3 CL E G H53099006OMIM:107250Anterior segment dysgenesis 16
HP:0012633HP:0012633Asymmetry of intraocular pressure0PRSS56 CL E G H64696039433OMIM:613517Microphthalmia, isolated 611
HP:0012633HP:0012633Asymmetry of intraocular pressure0PXDN CL E G H783714966OMIM:269400Corneal opacification with other ocular anomalies22
HP:0012633HP:0012633Asymmetry of intraocular pressure0SF3B1 CL E G H2345110768ORPHA:39044Uveal melanoma19
HP:0012633HP:0012633Asymmetry of intraocular pressure0SLC39A14 CL E G H2351620858OMIM:144755Hyperostosis cranialis interna5
HP:0012633HP:0012633Asymmetry of intraocular pressure0TEK CL E G H701011724OMIM:617272Glaucoma 3, primary congenital, E78
HP:0012633HP:0012633Asymmetry of intraocular pressure0VSX1 CL E G H3081312723OMIM:614195Craniofacial anomalies and anterior segment dysgenesis syndrome47
HP:0012633HP:0012633Asymmetry of intraocular pressure0VSX1 CL E G H3081312723ORPHA:98973Posterior polymorphous corneal dystrophy47
HP:0012633HP:0012633Asymmetry of intraocular pressure0ZEB1 CL E G H693511642ORPHA:98973Posterior polymorphous corneal dystrophy8
HP:0012633HP:0007906Ocular hypertension1ADAMTS17 CL E G H17069117109OMIM:613195Weill-Marchesani syndrome 4.214
HP:0012633HP:0007906Ocular hypertension1ASB10 CL E G H13637117185OMIM:603383GLAUCOMA 1, OPEN ANGLE, F; GLC1F54
HP:0012633HP:0007906Ocular hypertension1ASPH CL E G H444757OMIM:601552Facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs4
HP:0012633HP:0007906Ocular hypertension1BAP1 CL E G H8314950ORPHA:39044Uveal melanomaHP:0040283 - Occasional184
HP:0012633HP:0007906Ocular hypertension1C1QTNF5 CL E G H11490214344ORPHA:67042Late-onset retinal degenerationHP:0040284 - Very rare20
HP:0012633HP:0007906Ocular hypertension1CHST14 CL E G H11318924464ORPHA:2953Musculocontractural Ehlers-Danlos syndromeHP:0040282 - Frequent27
HP:0012633HP:0007906Ocular hypertension1COL18A1 CL E G H807812195OMIM:618880GLAUCOMA, PRIMARY CLOSED-ANGLE; GLCC177
HP:0012633HP:0007906Ocular hypertension1COL2A1 CL E G H12802200ORPHA:93315Spondylometaphyseal dysplasia, 'corner fracture' typeHP:0040284 - Very rare284
HP:0012633HP:0007906Ocular hypertension1COL8A2 CL E G H12962216ORPHA:98973Posterior polymorphous corneal dystrophyHP:0040284 - Very rare3
HP:0012633HP:0007906Ocular hypertension1CYP1B1 CL E G H15452597OMIM:231300Glaucoma 3, primary congenital, A.101
HP:0012633HP:0007906Ocular hypertension1CYP1B1 CL E G H15452597ORPHA:98977Juvenile glaucomaHP:0040282 - Frequent101
HP:0012633HP:0007906Ocular hypertension1CYSLTR2 CL E G H5710518274ORPHA:39044Uveal melanomaHP:0040283 - Occasional1
HP:0012633HP:0007906Ocular hypertension1DSE CL E G H2994021144ORPHA:2953Musculocontractural Ehlers-Danlos syndromeHP:0040282 - Frequent13
HP:0012633HP:0007906Ocular hypertension1EFEMP1 CL E G H22023218ORPHA:98977Juvenile glaucomaHP:0040282 - Frequent54
HP:0012633HP:0007906Ocular hypertension1FN1 CL E G H23353778ORPHA:93315Spondylometaphyseal dysplasia, 'corner fracture' typeHP:0040284 - Very rare9
HP:0012633HP:0007906Ocular hypertension1FOXE3 CL E G H23013808OMIM:610256Anterior segment dysgenesis 2.23
HP:0012633HP:0007906Ocular hypertension1GNA11 CL E G H27674379ORPHA:39044Uveal melanomaHP:0040283 - Occasional16
HP:0012633HP:0007906Ocular hypertension1GNAQ CL E G H27764390ORPHA:39044Uveal melanomaHP:0040283 - Occasional7
HP:0012633HP:0007906Ocular hypertension1GRHL2 CL E G H799772799ORPHA:98973Posterior polymorphous corneal dystrophyHP:0040284 - Very rare33
HP:0012633HP:0007906Ocular hypertension1HLA-A CL E G H31054931ORPHA:179Birdshot chorioretinopathyHP:0040281 - Very frequent4
HP:0012633HP:0007906Ocular hypertension1HMX1 CL E G H31665017OMIM:612109Oculoauricular syndrome.2
HP:0012633HP:0007906Ocular hypertension1LMX1B CL E G H40106654ORPHA:2614Nail-patella syndromeHP:0040283 - Occasional165
HP:0012633HP:0007906Ocular hypertension1LTBP2 CL E G H40536715OMIM:614819Weill-Marchesani syndrome 3.123
HP:0012633HP:0007906Ocular hypertension1MYOC CL E G H46537610ORPHA:98977Juvenile glaucomaHP:0040282 - Frequent47
HP:0012633HP:0007906Ocular hypertension1NFIA CL E G H47747784ORPHA:4019861p31p32 microdeletion syndrome12
HP:0012633HP:0007906Ocular hypertension1OVOL2 CL E G H5849515804ORPHA:98973Posterior polymorphous corneal dystrophyHP:0040284 - Very rare4
HP:0012633HP:0007906Ocular hypertension1PITX3 CL E G H53099006OMIM:107250Anterior segment dysgenesis 1.6
HP:0012633HP:0007906Ocular hypertension1PRSS56 CL E G H64696039433OMIM:613517Microphthalmia, isolated 6HP:0040284 - Very rare11
HP:0012633HP:0007906Ocular hypertension1PXDN CL E G H783714966OMIM:269400Corneal opacification with other ocular anomaliesHP:0040283 - Occasional22
HP:0012633HP:0007906Ocular hypertension1SF3B1 CL E G H2345110768ORPHA:39044Uveal melanomaHP:0040283 - Occasional19
HP:0012633HP:0007906Ocular hypertension1SLC39A14 CL E G H2351620858OMIM:144755Hyperostosis cranialis internaHP:0040284 - Very rare5
HP:0012633HP:0007906Ocular hypertension1TEK CL E G H701011724OMIM:617272Glaucoma 3, primary congenital, E.78
HP:0012633HP:0007906Ocular hypertension1VSX1 CL E G H3081312723OMIM:614195Craniofacial anomalies and anterior segment dysgenesis syndrome47
HP:0012633HP:0007906Ocular hypertension1VSX1 CL E G H3081312723ORPHA:98973Posterior polymorphous corneal dystrophyHP:0040284 - Very rare47
HP:0012633HP:0007906Ocular hypertension1ZEB1 CL E G H693511642ORPHA:98973Posterior polymorphous corneal dystrophyHP:0040284 - Very rare8


Genes (34) :ADAMTS17 ASB10 ASPH BAP1 C1QTNF5 CHST14 COL18A1 COL2A1 COL8A2 CYP1B1 CYSLTR2 DSE EFEMP1 FN1 FOXE3 GNA11 GNAQ GRHL2 HLA-A HMX1 LMX1B LOXL1 LTBP2 MYOC NFIA OVOL2 PITX3 PRSS56 PXDN SF3B1 SLC39A14 TEK VSX1 ZEB1

Diseases (24) :OMIM:613195 OMIM:603383 OMIM:601552 ORPHA:39044 ORPHA:67042 ORPHA:2953 OMIM:618880 ORPHA:93315 ORPHA:98973 OMIM:231300 ORPHA:98977 OMIM:610256 ORPHA:179 OMIM:612109 ORPHA:2614 OMIM:177650 OMIM:614819 ORPHA:401986 OMIM:107250 OMIM:613517 OMIM:269400 OMIM:144755 OMIM:617272 OMIM:614195
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.