Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of vision (HP:0000504)help
Parent Node:
expandVisual field defect (HP:0001123)help
..Starting node
..expandConstriction of peripheral visual field (HP:0001133)help
Term ID: 1133
Name: Constriction of peripheral visual field
Synonym: Concentric narrowing of visual field; Constricted visual field; Constricted visual fields; Limited peripheral vision; Reduced peripheral vision; Visual field constriction
Definition: An absolute or relative decrease in retinal sensitivity extending from edge (periphery) of the visual field in a concentric pattern. The visual field is the area that is perceived simultaneously by a fixating eye.
Comments:
Reference: HP:0001133
Genes and Diseases:
 
       Child Nodes:
........expandPeripheral visual field loss (HP:0007994) help
........expandPeripheral visual field constriction with >50 degrees central field preserved (HP:0030522) help
........expandPeripheral visual field constriction with 40-50 degrees central field preserved (HP:0030523) help
........expandPeripheral visual field constriction with 30-40 degrees central field preserved (HP:0030524) help
........expandPeripheral visual field constriction with 20-30 degrees central field preserved (HP:0030525) help
........expandPeripheral visual field constriction with 10-20 degrees central field preserved (HP:0030526) help
........expandPeripheral visual field constriction with <10 degrees central field preserved (HP:0030527) help

 Sister Nodes: 
..expandAbnormal visual field test (HP:0030588) help
..expandAltitudinal visual field defect (HP:0030531) help
..expandBlind-spot enlargment (HP:0030644) help
..expandGlaucomatous visual field defect (HP:0007854) help
..expandHemianopia (HP:0012377) help
..expandLarge central visual field defect (HP:0001129) help
..expandProgressive visual field defects (HP:0007987) help
..expandScotoma (HP:0000575) 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:0001133HP:0001133Constriction of peripheral visual field0ABCA4 CL E G H2434OMIM:604116CONE-ROD DYSTROPHY 3; CORD3826
HP:0001133HP:0001133Constriction of peripheral visual field0ABCA4 CL E G H2434OMIM:601718Retinitis pigmentosa 19826
HP:0001133HP:0001133Constriction of peripheral visual field0AGBL5 CL E G H6050926147OMIM:617023Retinitis pigmentosa 752
HP:0001133HP:0001133Constriction of peripheral visual field0AIPL1 CL E G H23746359OMIM:268000Retinitis pigmentosa.114
HP:0001133HP:0001133Constriction of peripheral visual field0AIRE CL E G H326360OMIM:240300AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I, WITH OR WITHOUT REVERSIBLE METAPHYSEAL DYSPLASIA; APS192
HP:0001133HP:0001133Constriction of peripheral visual field0ALMS1 CL E G H7840428OMIM:203800Alstrom syndrome.404
HP:0001133HP:0001133Constriction of peripheral visual field0AMACR CL E G H23600451OMIM:614307Alpha-methylacyl-CoA racemase deficiency44
HP:0001133HP:0001133Constriction of peripheral visual field0ARL3 CL E G H403694OMIM:618173RETINITIS PIGMENTOSA 83; RP831
HP:0001133HP:0001133Constriction of peripheral visual field0ARL6 CL E G H8410013210OMIM:209900Bardet-Biedl syndrome 129
HP:0001133HP:0001133Constriction of peripheral visual field0ARL6 CL E G H8410013210OMIM:268000Retinitis pigmentosa.29
HP:0001133HP:0001133Constriction of peripheral visual field0ARSG CL E G H2290124102OMIM:618144USHER SYNDROME, TYPE IV; USH4
HP:0001133HP:0001133Constriction of peripheral visual field0ATP6 CL E G H45087414ORPHA:644NARP syndromeHP:0040282 - Frequent
HP:0001133HP:0001133Constriction of peripheral visual field0BBS1 CL E G H582966OMIM:209900Bardet-Biedl syndrome 1114
HP:0001133HP:0001133Constriction of peripheral visual field0BBS2 CL E G H583967OMIM:616562Retinitis pigmentosa 74.97
HP:0001133HP:0001133Constriction of peripheral visual field0CACNA2D4 CL E G H9358920202OMIM:610478Retinal cone dystrophy 4.129
HP:0001133HP:0001133Constriction of peripheral visual field0CC2D2A CL E G H5754529253OMIM:619845RETINITIS PIGMENTOSA 93; RP93247
HP:0001133HP:0001133Constriction of peripheral visual field0CCDC28B CL E G H7914028163OMIM:209900Bardet-Biedl syndrome 14
HP:0001133HP:0001133Constriction of peripheral visual field0CDHR1 CL E G H9221114550OMIM:613660CONE-ROD DYSTROPHY 15; CORD15147
HP:0001133HP:0001133Constriction of peripheral visual field0CERKL CL E G H37529821699OMIM:608380Retinitis pigmentosa 2671
HP:0001133HP:0001133Constriction of peripheral visual field0CFAP418 CL E G H15765727232OMIM:617406Bardet-Biedl syndrome 21
HP:0001133HP:0001133Constriction of peripheral visual field0CFAP418 CL E G H15765727232OMIM:268000Retinitis pigmentosa.
HP:0001133HP:0001133Constriction of peripheral visual field0CHM CL E G H11211940OMIM:303100CHOROIDEREMIA.47
HP:0001133HP:0001133Constriction of peripheral visual field0CLRN1 CL E G H740112605OMIM:268000Retinitis pigmentosa.60
HP:0001133HP:0001133Constriction of peripheral visual field0CNGA1 CL E G H12592148OMIM:268000Retinitis pigmentosa.44
HP:0001133HP:0001133Constriction of peripheral visual field0CNGA1 CL E G H12592148OMIM:613756RETINITIS PIGMENTOSA 49; RP4944
HP:0001133HP:0001133Constriction of peripheral visual field0CNGB1 CL E G H12582151OMIM:613767Retinitis pigmentosa 45164
HP:0001133HP:0001133Constriction of peripheral visual field0CRX CL E G H14062383OMIM:120970Cone-Rod dystrophy 2158
HP:0001133HP:0001133Constriction of peripheral visual field0CRX CL E G H14062383OMIM:268000Retinitis pigmentosa.158
HP:0001133HP:0001133Constriction of peripheral visual field0CWC27 CL E G H1028310664OMIM:250410Retinitis pigmentosa with or without skeletal anomalies4
HP:0001133HP:0001133Constriction of peripheral visual field0CYP1B1 CL E G H15452597ORPHA:98977Juvenile glaucoma101
HP:0001133HP:0001133Constriction of peripheral visual field0CYP4V2 CL E G H28544023198OMIM:210370Bietti crystalline corneoretinal dystrophy.126
HP:0001133HP:0001133Constriction of peripheral visual field0CYP4V2 CL E G H28544023198ORPHA:41751Bietti crystalline dystrophyHP:0040282 - Frequent126
HP:0001133HP:0001133Constriction of peripheral visual field0DHDDS CL E G H7994720603OMIM:613861Retinitis pigmentosa 5947
HP:0001133HP:0001133Constriction of peripheral visual field0DLAT CL E G H17372896ORPHA:79244Pyruvate dehydrogenase E2 deficiency82
HP:0001133HP:0001133Constriction of peripheral visual field0EFEMP1 CL E G H22023218ORPHA:98977Juvenile glaucoma54
HP:0001133HP:0001133Constriction of peripheral visual field0ELOVL1 CL E G H6483414418OMIM:618527Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features
HP:0001133HP:0001133Constriction of peripheral visual field0EYS CL E G H34600721555OMIM:602772Retinitis pigmentosa 25209
HP:0001133HP:0001133Constriction of peripheral visual field0FAM161A CL E G H8414025808OMIM:606068RETINITIS PIGMENTOSA 28; RP2856
HP:0001133HP:0001133Constriction of peripheral visual field0GNAT1 CL E G H27794393OMIM:616389Night blindness, congenital stationary, type 1G39
HP:0001133HP:0001133Constriction of peripheral visual field0GUCY2D CL E G H30004689OMIM:601777Cone-Rod dystrophy 6124
HP:0001133HP:0001133Constriction of peripheral visual field0HGSNAT CL E G H13805026527OMIM:616544Retinitis pigmentosa 73.86
HP:0001133HP:0001133Constriction of peripheral visual field0HK1 CL E G H30984922OMIM:617460Retinitis pigmentosa 79.11
HP:0001133HP:0001133Constriction of peripheral visual field0HKDC1 CL E G H8020123302OMIM:619614RETINITIS PIGMENTOSA 92; RP922
HP:0001133HP:0001133Constriction of peripheral visual field0IDH3A CL E G H34195384OMIM:619007RETINITIS PIGMENTOSA 90; RP90
HP:0001133HP:0001133Constriction of peripheral visual field0IDH3B CL E G H34205385OMIM:612572RETINITIS PIGMENTOSA 46; RP4630
HP:0001133HP:0001133Constriction of peripheral visual field0IDS CL E G H34235389ORPHA:217093Mucopolysaccharidosis type 2, attenuated form86
HP:0001133HP:0001133Constriction of peripheral visual field0IDS CL E G H34235389ORPHA:217085Mucopolysaccharidosis type 2, severe form86
HP:0001133HP:0001133Constriction of peripheral visual field0IFT140 CL E G H974229077OMIM:266920Short-rib thoracic dysplasia 9 with or without polydactyly148
HP:0001133HP:0001133Constriction of peripheral visual field0IFT172 CL E G H2616030391OMIM:619471BARDET-BIEDL SYNDROME 20; BBS2048
HP:0001133HP:0001133Constriction of peripheral visual field0IMPDH1 CL E G H36146052OMIM:180105Retinitis pigmentosa 10.52
HP:0001133HP:0001133Constriction of peripheral visual field0KIF3B CL E G H93716320OMIM:618955RETINITIS PIGMENTOSA 89; RP89
HP:0001133HP:0001133Constriction of peripheral visual field0KIZ CL E G H5585715865OMIM:615780Retinitis pigmentosa 69.3
HP:0001133HP:0001133Constriction of peripheral visual field0LCA5 CL E G H16769131923ORPHA:364055Severe early-childhood-onset retinal dystrophy70
HP:0001133HP:0001133Constriction of peripheral visual field0LRAT CL E G H92276685OMIM:268000Retinitis pigmentosa.62
HP:0001133HP:0001133Constriction of peripheral visual field0LRAT CL E G H92276685ORPHA:364055Severe early-childhood-onset retinal dystrophy62
HP:0001133HP:0001133Constriction of peripheral visual field0MERTK CL E G H104617027OMIM:613862Retinitis pigmentosa 3875
HP:0001133HP:0001133Constriction of peripheral visual field0MYOC CL E G H46537610ORPHA:98977Juvenile glaucoma47
HP:0001133HP:0001133Constriction of peripheral visual field0OAT CL E G H49428091ORPHA:414Gyrate atrophy of choroid and retinaHP:0040282 - Frequent94
HP:0001133HP:0001133Constriction of peripheral visual field0OFD1 CL E G H84812567OMIM:300424Retinitis pigmentosa 23201
HP:0001133HP:0001133Constriction of peripheral visual field0OPA1 CL E G H49768140ORPHA:1215Autosomal dominant optic atrophy plus syndromeHP:0040283 - Occasional214
HP:0001133HP:0001133Constriction of peripheral visual field0PDE6A CL E G H51458785OMIM:613810RETINITIS PIGMENTOSA 43; RP43116
HP:0001133HP:0001133Constriction of peripheral visual field0PDE6G CL E G H51488789OMIM:268000Retinitis pigmentosa.18
HP:0001133HP:0001133Constriction of peripheral visual field0PDE6G CL E G H51488789OMIM:613582Retinitis pigmentosa 5718
HP:0001133HP:0001133Constriction of peripheral visual field0PEX1 CL E G H51898850ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent169
HP:0001133HP:0001133Constriction of peripheral visual field0PEX10 CL E G H51928851ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent75
HP:0001133HP:0001133Constriction of peripheral visual field0PEX11B CL E G H87998853ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent4
HP:0001133HP:0001133Constriction of peripheral visual field0PEX12 CL E G H51938854ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent65
HP:0001133HP:0001133Constriction of peripheral visual field0PEX13 CL E G H51948855ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent66
HP:0001133HP:0001133Constriction of peripheral visual field0PEX14 CL E G H51958856ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent46
HP:0001133HP:0001133Constriction of peripheral visual field0PEX16 CL E G H94098857ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent59
HP:0001133HP:0001133Constriction of peripheral visual field0PEX19 CL E G H58249713ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent62
HP:0001133HP:0001133Constriction of peripheral visual field0PEX2 CL E G H58289717ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent82
HP:0001133HP:0001133Constriction of peripheral visual field0PEX26 CL E G H5567022965ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent106
HP:0001133HP:0001133Constriction of peripheral visual field0PEX3 CL E G H85048858ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent47
HP:0001133HP:0001133Constriction of peripheral visual field0PEX5 CL E G H58309719ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent99
HP:0001133HP:0001133Constriction of peripheral visual field0PEX6 CL E G H51908859ORPHA:772Infantile Refsum diseaseHP:0040281 - Very frequent98
HP:0001133HP:0001133Constriction of peripheral visual field0POC1B CL E G H28280930836OMIM:615973Cone-Rod dystrophy 20.3
HP:0001133HP:0001133Constriction of peripheral visual field0POMGNT1 CL E G H5562419139OMIM:617123RETINITIS PIGMENTOSA 76; RP76180
HP:0001133HP:0001133Constriction of peripheral visual field0POU3F4 CL E G H54569217ORPHA:1435Xq21 microdeletion syndrome40
HP:0001133HP:0001133Constriction of peripheral visual field0PROM1 CL E G H88429454OMIM:612095RETINITIS PIGMENTOSA 41; RP41110
HP:0001133HP:0001133Constriction of peripheral visual field0PRPF31 CL E G H2612115446OMIM:600138Retinitis pigmentosa 1170
HP:0001133HP:0001133Constriction of peripheral visual field0PRPF8 CL E G H1059417340OMIM:600059Retinitis pigmentosa 13.94
HP:0001133HP:0001133Constriction of peripheral visual field0PRPH2 CL E G H59619942OMIM:608133Retinitis pigmentosa 7.159
HP:0001133HP:0001133Constriction of peripheral visual field0PRPH2 CL E G H59619942ORPHA:52427Retinitis punctata albescens159
HP:0001133HP:0001133Constriction of peripheral visual field0RAX2 CL E G H8483918286OMIM:62010252
HP:0001133HP:0001133Constriction of peripheral visual field0RBP3 CL E G H59499921OMIM:268000Retinitis pigmentosa.108
HP:0001133HP:0001133Constriction of peripheral visual field0RBP3 CL E G H59499921OMIM:615233Retinitis pigmentosa 66.108
HP:0001133HP:0001133Constriction of peripheral visual field0RDH11 CL E G H5110917964ORPHA:436245Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndromeHP:0040282 - Frequent2
HP:0001133HP:0001133Constriction of peripheral visual field0RDH5 CL E G H59599940ORPHA:52427Retinitis punctata albescens32
HP:0001133HP:0001133Constriction of peripheral visual field0RGR CL E G H59959990OMIM:613769RETINITIS PIGMENTOSA 44; RP4428
HP:0001133HP:0001133Constriction of peripheral visual field0RHO CL E G H601010012ORPHA:52427Retinitis punctata albescens107
HP:0001133HP:0001133Constriction of peripheral visual field0RLBP1 CL E G H601710024ORPHA:52427Retinitis punctata albescens47
HP:0001133HP:0001133Constriction of peripheral visual field0RNU4ATAC CL E G H10015168334016OMIM:226960EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS15
HP:0001133HP:0001133Constriction of peripheral visual field0ROM1 CL E G H609410254OMIM:268000Retinitis pigmentosa.38
HP:0001133HP:0001133Constriction of peripheral visual field0ROM1 CL E G H609410254OMIM:608133Retinitis pigmentosa 7.38
HP:0001133HP:0001133Constriction of peripheral visual field0RP1 CL E G H610110263OMIM:180100Retinitis pigmentosa 1.111
HP:0001133HP:0001133Constriction of peripheral visual field0RP2 CL E G H610210274OMIM:312600Retinitis pigmentosa 2, X-linked.45
HP:0001133HP:0001133Constriction of peripheral visual field0RP9 CL E G H610010288OMIM:180104Retinitis pigmentosa 9.14
HP:0001133HP:0001133Constriction of peripheral visual field0RPE65 CL E G H612110294OMIM:618697RETINITIS PIGMENTOSA 87 WITH CHOROIDAL INVOLVEMENT; RP87129
HP:0001133HP:0001133Constriction of peripheral visual field0RPE65 CL E G H612110294ORPHA:364055Severe early-childhood-onset retinal dystrophy129
HP:0001133HP:0001133Constriction of peripheral visual field0RPGR CL E G H610310295OMIM:300029Retinitis pigmentosa 3200
HP:0001133HP:0001133Constriction of peripheral visual field0RRM2B CL E G H5048417296OMIM:268315ROD-CONE DYSTROPHY, SENSORINEURAL DEAFNESS, AND FANCONI-TYPE RENAL DYSFUNCTION125
HP:0001133HP:0001133Constriction of peripheral visual field0SDHA CL E G H638910680OMIM:619259NEURODEGENERATION WITH ATAXIA AND LATE-ONSET OPTIC ATROPHY; NDAXOA304
HP:0001133HP:0001133Constriction of peripheral visual field0SEMA4A CL E G H6421810729OMIM:610283Cone-Rod dystrophy 1048
HP:0001133HP:0001133Constriction of peripheral visual field0SH3BP2 CL E G H645210825OMIM:118400Cherubism177
HP:0001133HP:0001133Constriction of peripheral visual field0SH3TC2 CL E G H7962829427ORPHA:99949Charcot-Marie-Tooth disease type 4C493
HP:0001133HP:0001133Constriction of peripheral visual field0SLC6A6 CL E G H653311052OMIM:145350Hypotaurinemic retinal degeneration and cardiomyopathy
HP:0001133HP:0001133Constriction of peripheral visual field0SOST CL E G H5096413771OMIM:269500Sclerosteosis 1.26
HP:0001133HP:0001133Constriction of peripheral visual field0SPATA7 CL E G H5581220423OMIM:604232LEBER CONGENITAL AMAUROSIS 3; LCA348
HP:0001133HP:0001133Constriction of peripheral visual field0SPATA7 CL E G H5581220423ORPHA:364055Severe early-childhood-onset retinal dystrophy48
HP:0001133HP:0001133Constriction of peripheral visual field0TIMM8A CL E G H167811817OMIM:304700Mohr-Tranebjaerg syndrome.15
HP:0001133HP:0001133Constriction of peripheral visual field0TMEM126A CL E G H8423325382OMIM:612989Optic atrophy 7 with or without auditory neuropathy.23
HP:0001133HP:0001133Constriction of peripheral visual field0TULP1 CL E G H728712423OMIM:613843Leber congenital amaurosis 15.66
HP:0001133HP:0001133Constriction of peripheral visual field0TULP1 CL E G H728712423OMIM:600132RETINITIS PIGMENTOSA 14; RP1466
HP:0001133HP:0001133Constriction of peripheral visual field0YARS1 CL E G H856512840OMIM:619418NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 2; IMNEPD2
HP:0001133HP:0001133Constriction of peripheral visual field0ZNF408 CL E G H7979720041OMIM:616469Retinitis pigmentosa 72.14
HP:0001133HP:0001133Constriction of peripheral visual field0ZNF513 CL E G H13055726498OMIM:613617Retinitis pigmentosa 5827
HP:0001133HP:0030527Very severe constriction of peripheral visual field1 CL E G H
HP:0001133HP:0030526Severe constriction of peripheral visual field1 CL E G H
HP:0001133HP:0030525Moderate constriction of peripheral visual field1 CL E G H
HP:0001133HP:0030522Mild constriction of peripheral visual field1 CL E G H
HP:0001133HP:0007994Peripheral visual field loss1ABCA4 CL E G H2434OMIM:604116CONE-ROD DYSTROPHY 3; CORD3826
HP:0001133HP:0007994Peripheral visual field loss1AGBL5 CL E G H6050926147OMIM:617023Retinitis pigmentosa 75.2
HP:0001133HP:0007994Peripheral visual field loss1ARL6 CL E G H8410013210OMIM:209900Bardet-Biedl syndrome 129
HP:0001133HP:0007994Peripheral visual field loss1BBS1 CL E G H582966OMIM:209900Bardet-Biedl syndrome 1114
HP:0001133HP:0007994Peripheral visual field loss1CCDC28B CL E G H7914028163OMIM:209900Bardet-Biedl syndrome 14
HP:0001133HP:0007994Peripheral visual field loss1CNGA1 CL E G H12592148OMIM:613756RETINITIS PIGMENTOSA 49; RP4944
HP:0001133HP:0007994Peripheral visual field loss1CNGB1 CL E G H12582151OMIM:613767Retinitis pigmentosa 45.164
HP:0001133HP:0007994Peripheral visual field loss1CRX CL E G H14062383OMIM:120970Cone-Rod dystrophy 2.158
HP:0001133HP:0007994Peripheral visual field loss1CWC27 CL E G H1028310664OMIM:250410Retinitis pigmentosa with or without skeletal anomalies4
HP:0001133HP:0007994Peripheral visual field loss1CYP1B1 CL E G H15452597ORPHA:98977Juvenile glaucomaHP:0040282 - Frequent101
HP:0001133HP:0007994Peripheral visual field loss1DLAT CL E G H17372896ORPHA:79244Pyruvate dehydrogenase E2 deficiencyHP:0040283 - Occasional82
HP:0001133HP:0007994Peripheral visual field loss1EFEMP1 CL E G H22023218ORPHA:98977Juvenile glaucomaHP:0040282 - Frequent54
HP:0001133HP:0007994Peripheral visual field loss1GUCY2D CL E G H30004689OMIM:601777Cone-Rod dystrophy 6.124
HP:0001133HP:0007994Peripheral visual field loss1IDS CL E G H34235389ORPHA:217093Mucopolysaccharidosis type 2, attenuated formHP:0040283 - Occasional86
HP:0001133HP:0007994Peripheral visual field loss1IDS CL E G H34235389ORPHA:217085Mucopolysaccharidosis type 2, severe formHP:0040283 - Occasional86
HP:0001133HP:0007994Peripheral visual field loss1IFT140 CL E G H974229077OMIM:266920Short-rib thoracic dysplasia 9 with or without polydactyly148
HP:0001133HP:0007994Peripheral visual field loss1LCA5 CL E G H16769131923ORPHA:364055Severe early-childhood-onset retinal dystrophyHP:0040282 - Frequent70
HP:0001133HP:0007994Peripheral visual field loss1LRAT CL E G H92276685ORPHA:364055Severe early-childhood-onset retinal dystrophyHP:0040282 - Frequent62
HP:0001133HP:0007994Peripheral visual field loss1MYOC CL E G H46537610ORPHA:98977Juvenile glaucomaHP:0040282 - Frequent47
HP:0001133HP:0007994Peripheral visual field loss1PDE6A CL E G H51458785OMIM:613810RETINITIS PIGMENTOSA 43; RP43116
HP:0001133HP:0007994Peripheral visual field loss1POU3F4 CL E G H54569217ORPHA:1435Xq21 microdeletion syndromeHP:0040282 - Frequent40
HP:0001133HP:0007994Peripheral visual field loss1PROM1 CL E G H88429454OMIM:612095RETINITIS PIGMENTOSA 41; RP41110
HP:0001133HP:0007994Peripheral visual field loss1PRPH2 CL E G H59619942ORPHA:52427Retinitis punctata albescensHP:0040282 - Frequent159
HP:0001133HP:0007994Peripheral visual field loss1RDH5 CL E G H59599940ORPHA:52427Retinitis punctata albescensHP:0040282 - Frequent32
HP:0001133HP:0007994Peripheral visual field loss1RHO CL E G H601010012ORPHA:52427Retinitis punctata albescensHP:0040282 - Frequent107
HP:0001133HP:0007994Peripheral visual field loss1RLBP1 CL E G H601710024ORPHA:52427Retinitis punctata albescensHP:0040282 - Frequent47
HP:0001133HP:0007994Peripheral visual field loss1RNU4ATAC CL E G H10015168334016OMIM:226960EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS15
HP:0001133HP:0007994Peripheral visual field loss1RPE65 CL E G H612110294OMIM:618697RETINITIS PIGMENTOSA 87 WITH CHOROIDAL INVOLVEMENT; RP87129
HP:0001133HP:0007994Peripheral visual field loss1RPE65 CL E G H612110294ORPHA:364055Severe early-childhood-onset retinal dystrophyHP:0040282 - Frequent129
HP:0001133HP:0007994Peripheral visual field loss1RRM2B CL E G H5048417296OMIM:268315ROD-CONE DYSTROPHY, SENSORINEURAL DEAFNESS, AND FANCONI-TYPE RENAL DYSFUNCTION125
HP:0001133HP:0007994Peripheral visual field loss1SDHA CL E G H638910680OMIM:619259NEURODEGENERATION WITH ATAXIA AND LATE-ONSET OPTIC ATROPHY; NDAXOA304
HP:0001133HP:0007994Peripheral visual field loss1SEMA4A CL E G H6421810729OMIM:610283Cone-Rod dystrophy 10.48
HP:0001133HP:0007994Peripheral visual field loss1SH3TC2 CL E G H7962829427ORPHA:99949Charcot-Marie-Tooth disease type 4CHP:0040284 - Very rare493
HP:0001133HP:0007994Peripheral visual field loss1SLC6A6 CL E G H653311052OMIM:145350Hypotaurinemic retinal degeneration and cardiomyopathy
HP:0001133HP:0007994Peripheral visual field loss1SPATA7 CL E G H5581220423ORPHA:364055Severe early-childhood-onset retinal dystrophyHP:0040282 - Frequent48
HP:0001133HP:0007994Peripheral visual field loss1ZNF513 CL E G H13055726498OMIM:613617Retinitis pigmentosa 58.27


Genes (102) :ABCA4 AGBL5 AIPL1 AIRE ALMS1 AMACR ARL3 ARL6 ARSG ATP6 BBS1 BBS2 CACNA2D4 CC2D2A CCDC28B CDHR1 CERKL CFAP418 CHM CLRN1 CNGA1 CNGB1 CRX CWC27 CYP1B1 CYP4V2 DHDDS DLAT EFEMP1 ELOVL1 EYS FAM161A GNAT1 GUCY2D HGSNAT HK1 HKDC1 IDH3A IDH3B IDS IFT140 IFT172 IMPDH1 KIF3B KIZ LCA5 LRAT MERTK MYOC OAT OFD1 OPA1 PDE6A PDE6G PEX1 PEX10 PEX11B PEX12 PEX13 PEX14 PEX16 PEX19 PEX2 PEX26 PEX3 PEX5 PEX6 POC1B POMGNT1 POU3F4 PROM1 PRPF31 PRPF8 PRPH2 RAX2 RBP3 RDH11 RDH5 RGR RHO RLBP1 RNU4ATAC ROM1 RP1 RP2 RP9 RPE65 RPGR RRM2B SDHA SEMA4A SH3BP2 SH3TC2 SLC6A6 SOST SPATA7 TIMM8A TMEM126A TULP1 YARS1 ZNF408 ZNF513

Diseases (85) :OMIM:604116 OMIM:601718 OMIM:617023 OMIM:268000 OMIM:240300 OMIM:203800 OMIM:614307 OMIM:618173 OMIM:209900 OMIM:618144 ORPHA:644 OMIM:616562 OMIM:610478 OMIM:619845 OMIM:613660 OMIM:608380 OMIM:617406 OMIM:303100 OMIM:613756 OMIM:613767 OMIM:120970 OMIM:250410 ORPHA:98977 OMIM:210370 ORPHA:41751 OMIM:613861 ORPHA:79244 OMIM:618527 OMIM:602772 OMIM:606068 OMIM:616389 OMIM:601777 OMIM:616544 OMIM:617460 OMIM:619614 OMIM:619007 OMIM:612572 ORPHA:217093 ORPHA:217085 OMIM:266920 OMIM:619471 OMIM:180105 OMIM:618955 OMIM:615780 ORPHA:364055 OMIM:613862 ORPHA:414 OMIM:300424 ORPHA:1215 OMIM:613810 OMIM:613582 ORPHA:772 OMIM:615973 OMIM:617123 ORPHA:1435 OMIM:612095 OMIM:600138 OMIM:600059 OMIM:608133 ORPHA:52427 OMIM:620102 OMIM:615233 ORPHA:436245 OMIM:613769 OMIM:226960 OMIM:180100 OMIM:312600 OMIM:180104 OMIM:618697 OMIM:300029 OMIM:268315 OMIM:619259 OMIM:610283 OMIM:118400 ORPHA:99949 OMIM:145350 OMIM:269500 OMIM:604232 OMIM:304700 OMIM:612989 OMIM:613843 OMIM:600132 OMIM:619418 OMIM:616469 OMIM:613617
 

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