Myopia
Symptom Information:
Symptom ID: | HPO:0000545 | ||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the eye(HPO:0000478) Abnormal eye physiology(HPO:0012373) Abnormality of refraction(HPO:0000539) Myopia(HPO:0000545) MedDRA: Eye disorders(MedDRA:10015919) Vision disorders(MedDRA:10047518) Refractive and accommodative disorders(MedDRA:10038267) Myopia(HPO:0000545) |
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Database Frequency: | 286 / 7739 | ||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
16p11.2p12.2 microduplication syndrome | (Orphanet:261204) |
16q24.3 microdeletion syndrome | (Orphanet:261250) |
19p13.12 microdeletion syndrome | (Orphanet:254346) |
1p36 deletion syndrome | (Orphanet:1606) |
2q23.1 microdeletion syndrome | (Orphanet:228402) |
3q13 microdeletion syndrome | (Orphanet:1621) |
49,XXXXY syndrome | (Orphanet:96264) |
5q35 microduplication syndrome | (Orphanet:228415) |
6q16 deletion syndrome | (Orphanet:171829) |
ALDH18A1-related De Barsy syndrome | (Orphanet:35664) |
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES | (OMIM:300887) |
Ablepharon macrostomia syndrome | (Orphanet:920) |
Acro-pectoro-renal dysplasia | (Orphanet:956) |
Acrocraniofacial dysostosis | (Orphanet:949) |
Acromelic frontonasal dysplasia | (Orphanet:1827) |
Acroosteolysis, dominant type | (Orphanet:955) |
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
Alopecia - contractures - dwarfism - intellectual deficit | (Orphanet:1005) |
Alpha-mannosidosis | (Orphanet:61) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Alport syndrome | (Orphanet:63) |
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis | (Orphanet:86818) |
Angelman syndrome | (Orphanet:72) |
Aniridia - ptosis - intellectual deficit - familial obesity | (Orphanet:1067) |
Anophthalmia - megalocornea - cardiopathy - skeletal anomalies | (Orphanet:1101) |
Aplasia cutis - myopia | (Orphanet:1117) |
Aplasia cutis congenita - intestinal lymphangiectasia | (Orphanet:1116) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Auriculoocular anomalies - cleft lip | (Orphanet:71270) |
Autosomal dominant nonsyndromic intellectual deficit | (Orphanet:178469) |
Autosomal dominant rhegmatogenous retinal detachment | (Orphanet:209867) |
Autosomal recessive Alport syndrome | (Orphanet:88919) |
Autosomal recessive Stickler syndrome | (Orphanet:250984) |
Autosomal recessive cutis laxa type 2 | (Orphanet:90350) |
Autosomal recessive cutis laxa type 2, classic type | (Orphanet:357074) |
Autosomal recessive cutis laxa type 2A | (Orphanet:357058) |
Autosomal recessive limb-girdle muscular dystrophy type 2O | (Orphanet:206564) |
Autosomal recessive limb-girdle muscular dystrophy type 2S | (Orphanet:369840) |
Autosomal recessive spastic paraplegia type 45 | (Orphanet:320396) |
BRITTLE CORNEA SYNDROME 1 | (OMIM:229200) |
BRITTLE CORNEA SYNDROME 2 | (OMIM:614170) |
Baller-Gerold syndrome | (Orphanet:1225) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Bardet-Biedl syndrome 9 | (OMIM:615986) |
Biotinidase deficiency | (Orphanet:79241) |
Blepharophimosis - epicanthus inversus - ptosis | (Orphanet:126) |
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency | (Orphanet:329255) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Blepharoptosis - myopia - ectopia lentis | (Orphanet:1259) |
Blue cone monochromatism | (Orphanet:16) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
Brittle cornea syndrome | (Orphanet:90354) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CARDIOFACIOCUTANEOUS SYNDROME 2 | (OMIM:615278) |
CARDIOFACIOCUTANEOUS SYNDROME 4 | (OMIM:615280) |
CATARACT 42 | (OMIM:115900) |
CATARACT 6, MULTIPLE TYPES | (OMIM:116600) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
CONE-ROD DYSTROPHY, X-LINKED, 1 | (OMIM:304020) |
CONE-ROD DYSTROPHY, X-LINKED, 3 | (OMIM:300476) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
CORNELIA DE LANGE SYNDROME 3 | (OMIM:610759) |
CORNELIA DE LANGE SYNDROME 5 | (OMIM:300882) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cataract-microcornea syndrome | (Orphanet:1377) |
Char syndrome | (Orphanet:46627) |
Choroideremia | (Orphanet:180) |
Classical homocystinuria | (Orphanet:394) |
Coffin-Siris syndrome | (Orphanet:1465) |
Cohen syndrome | (Orphanet:193) |
Conductive deafness - ptosis - skeletal anomalies | (Orphanet:3236) |
Cone dystrophy with supernormal rod response | (Orphanet:209932) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Congenital microcoria | (Orphanet:566) |
Connective tissue disorder due to lysyl hydroxylase-3 deficiency | (Orphanet:300284) |
Cornelia de Lange syndrome | (Orphanet:199) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
Costello syndrome | (Orphanet:3071) |
Cowden syndrome | (Orphanet:201) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Craniosynostosis, Boston type | (Orphanet:1541) |
De Barsy syndrome | (Orphanet:2962) |
Deafness - epiphyseal dysplasia - short stature | (Orphanet:3218) |
Deafness - intellectual deficit, Martin-Probst type | (Orphanet:85321) |
Deafness - onychodystrophy | (Orphanet:3231) |
Desbuquois syndrome | (Orphanet:1425) |
Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type | (Orphanet:363444) |
Distal limb deficiencies - micrognathia syndrome | (Orphanet:1307) |
Donnai-Barrow syndrome | (Orphanet:2143) |
Down syndrome | (Orphanet:870) |
Dubowitz syndrome | (Orphanet:235) |
Dwarfism - intellectual deficit - eye abnormality | (Orphanet:2650) |
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 | (OMIM:601776) |
Ectopia lentis - chorioretinal dystrophy - myopia | (Orphanet:1884) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type | (Orphanet:300179) |
Ehlers-Danlos syndrome, kyphoscoliotic type | (Orphanet:1900) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
Emanuel syndrome | (Orphanet:96170) |
Encephalopathy due to sulfite oxidase deficiency | (Orphanet:833) |
Epidermolysis bullosa simplex with anodontia/hypodontia | (Orphanet:2325) |
FRONTOOCULAR SYNDROME | (OMIM:605321) |
FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM | (OMIM:264420) |
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation | (Orphanet:1970) |
Familial dysautonomia | (Orphanet:1764) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis | (Orphanet:31043) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement | (Orphanet:2196) |
Familial vascular leukoencephalopathy | (Orphanet:36383) |
Flynn-Aird syndrome | (Orphanet:2047) |
GAPO syndrome | (Orphanet:2067) |
GLAUCOMA 1, OPEN ANGLE, A | (OMIM:137750) |
GLAUCOMA, PRIMARY OPEN ANGLE | (OMIM:137760) |
GLAUCOMA-RELATED PIGMENT DISPERSION SYNDROME | (OMIM:600510) |
Gastrocutaneous syndrome | (Orphanet:2069) |
Gaucher disease type 3 | (Orphanet:77261) |
Gyrate atrophy of choroid and retina | (Orphanet:414) |
HUNTER-MACDONALD SYNDROME | (OMIM:611962) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Helicoid peripapillary chorioretinal degeneration | (Orphanet:86813) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Hermansky-Pudlak syndrome | (Orphanet:79430) |
High myopia-sensorineural deafness syndrome | (Orphanet:363396) |
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly | (Orphanet:2180) |
Hypertryptophanemia | (Orphanet:2224) |
ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS | (OMIM:242150) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Intellectual deficit - myopathy - short stature - endocrine defect | (Orphanet:3068) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Intellectual deficit, X-linked, Brooks type | (Orphanet:3056) |
Ito hypomelanosis | (Orphanet:435) |
Juvenile glaucoma | (Orphanet:98977) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Kniest dysplasia | (Orphanet:485) |
Knobloch syndrome | (Orphanet:1571) |
Kozlowski-Brown-Hardwick syndrome | (Orphanet:2352) |
LAMB-2-related infantile-onset nephrotic syndrome | (Orphanet:306507) |
LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM | (OMIM:614381) |
Leber congenital amaurosis 15 | (OMIM:613843) |
Leukoencephalopathy - ataxia - hypodontia - hypomyelination | (Orphanet:137639) |
Lhermitte-Duclos disease | (Orphanet:65285) |
MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE | (OMIM:248000) |
MARFANOID HABITUS WITH SITUS INVERSUS | (OMIM:609008) |
MICROPHTHALMIA, ISOLATED, WITH CORECTOPIA | (OMIM:156900) |
MICROSPHEROPHAKIA WITH HERNIA | (OMIM:157150) |
MUCOLIPIDOSIS III GAMMA | (OMIM:252605) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 11 | (OMIM:615181) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 | (OMIM:613150) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 | (OMIM:253280) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 | (OMIM:253800) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 5 | (OMIM:613153) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1 | (OMIM:613155) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 | (OMIM:613156) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3 | (OMIM:613151) |
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY | (OMIM:601347) |
MYOPIA 1, X-LINKED | (OMIM:310460) |
MYOPIA 10 | (OMIM:609259) |
MYOPIA 15, AUTOSOMAL DOMINANT | (OMIM:612717) |
MYOPIA 18, AUTOSOMAL RECESSIVE | (OMIM:255500) |
MYOPIA 22, AUTOSOMAL DOMINANT | (OMIM:615420) |
MYOPIA 24, AUTOSOMAL DOMINANT | (OMIM:615946) |
MYOPIA 7 | (OMIM:609256) |
MYOPIA 8 | (OMIM:609257) |
MYOPIA 9 | (OMIM:609258) |
Marfan syndrome | (Orphanet:558) |
Marfan syndrome type 1 | (Orphanet:284963) |
Marfanoid syndrome, De Silva type | (Orphanet:2464) |
Marshall syndrome | (Orphanet:560) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
Mesomelic dwarfism, Reinhardt-Pfeiffer type | (Orphanet:2634) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Microcornea - corectopia - macular hypoplasia | (Orphanet:2535) |
Microphthalmia with brain and digit anomalies | (Orphanet:139471) |
Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
Microspherophakia - metaphyseal dysplasia | (Orphanet:2551) |
Mohr-Tranebjaerg syndrome | (Orphanet:52368) |
Monosomy 5p | (Orphanet:281) |
Monosomy 9p | (Orphanet:261112) |
Mucopolysaccharidosis type 3 | (Orphanet:581) |
Multiple epiphyseal dysplasia | (Orphanet:251) |
Multiple epiphyseal dysplasia, Beighton type | (Orphanet:166011) |
Multiple non-ossifying fibromatosis | (Orphanet:2029) |
Muscle-eye-brain disease | (Orphanet:588) |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B | (OMIM:257270) |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C | (OMIM:613216) |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F | (OMIM:615058) |
NOONAN SYNDROME 1 | (OMIM:163950) |
NOONAN SYNDROME 6 | (OMIM:613224) |
Neuroectodermal melanolysosomal disease | (Orphanet:33445) |
Night blindness - skeletal anomalies - dysmorphism | (Orphanet:1390) |
Noonan syndrome | (Orphanet:648) |
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE | (OMIM:257850) |
OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA | (OMIM:311000) |
Oculo-skeletal-renal syndrome | (Orphanet:2716) |
Oculocerebral hypopigmentation syndrome, Cross type | (Orphanet:2719) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |
Oculocutaneous albinism | (Orphanet:55) |
Oculocutaneous albinism type 1 | (Orphanet:352731) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Oculoosteocutaneous syndrome | (Orphanet:2713) |
Ophthalmoplegia - intellectual deficit - lingua scrotalis | (Orphanet:2743) |
Osteopenia - myopia - hearing loss - intellectual deficit - facial dysmorphism | (Orphanet:91133) |
PORETTI-BOLTSHAUSER SYNDROME | (OMIM:615960) |
PSEUDOXANTHOMA ELASTICUM, FORME FRUSTEPSEUDOXANTHOMA ELASTICUM, HETEROZYGOUS, INCLUDED | (OMIM:177850) |
Partial congenital cataract | (Orphanet:98992) |
Pelizaeus-Merzbacher-like due to GJC2 mutation | (Orphanet:280282) |
Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
Peters-plus syndrome | (Orphanet:709) |
Pilodental dysplasia - refractive errors | (Orphanet:2892) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Polydactyly-myopia syndrome | (Orphanet:2917) |
Pontocerebellar hypoplasia type 8 | (Orphanet:324569) |
Prader-Willi syndrome | (Orphanet:739) |
Progressive bifocal chorioretinal atrophy | (Orphanet:75373) |
Proteus syndrome | (Orphanet:744) |
Proteus-like syndrome | (Orphanet:2969) |
Proximal 16p11.2 microdeletion syndrome | (Orphanet:261197) |
Pseudoxanthoma elasticum | (Orphanet:758) |
RETINAL DYSTROPHY AND OBESITY | (OMIM:616188) |
RETINITIS PIGMENTOSA 2 | (OMIM:312600) |
RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION | (OMIM:268050) |
Rare isolated myopia | (Orphanet:98619) |
Renal coloboma syndrome | (Orphanet:1475) |
Renal-genital-middle ear anomalies | (Orphanet:1092) |
Retinal degeneration - nanophthalmos - glaucoma | (Orphanet:1574) |
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion | (Orphanet:353281) |
SCHAAF-YANG SYNDROME | (OMIM:615547) |
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY | (OMIM:614800) |
SHORT syndrome | (Orphanet:3163) |
STICKLER SYNDROME, TYPE I | (OMIM:108300) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Short-rib thoracic dysplasia 5 with or without polydactyly | (OMIM:614376) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Singleton-Merten dysplasia | (Orphanet:85191) |
Sinus node disease and myopia | (OMIM:182190) |
Sjögren-Larsson syndrome | (Orphanet:816) |
Smith-Magenis syndrome | (Orphanet:819) |
Spastic ataxia - corneal dystrophy | (Orphanet:2572) |
Spondylo-ocular syndrome | (Orphanet:85194) |
Spondyloepimetaphyseal dysplasia congenita, Strudwick type | (Orphanet:93346) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia | (Orphanet:253) |
Spondyloepiphyseal dysplasia congenita | (Orphanet:94068) |
Spondyloepiphyseal dysplasia, MacDermot type | (Orphanet:163668) |
Spondylometaphyseal dysplasia - cone-rod dystrophy | (Orphanet:85167) |
Spondylometaphyseal dysplasia, Schmidt type | (Orphanet:93316) |
Stickler syndrome | (Orphanet:828) |
Stickler syndrome type 1 | (Orphanet:90653) |
Stickler syndrome type 2 | (Orphanet:90654) |
Syndactyly - telecanthus - anogenital and renal malformations | (Orphanet:140952) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
Temtamy syndrome | (Orphanet:1777) |
Timothy syndrome | (Orphanet:65283) |
Usher syndrome | (Orphanet:886) |
Usher syndrome type 2 | (Orphanet:231178) |
VAN BOGAERT-HOZAY SYNDROME | (OMIM:277150) |
Van den Bosch syndrome | (Orphanet:3417) |
WEILL-MARCHESANI SYNDROME 3 | (OMIM:614819) |
Wagner disease | (Orphanet:898) |
Weill-Marchesani syndrome | (Orphanet:3449) |
White forelock with malformations | (Orphanet:2475) |
Williams syndrome | (Orphanet:904) |
Wrinkly skin syndrome | (Orphanet:2834) |
X-linked Alport syndrome | (Orphanet:88917) |
X-linked intellectual deficit, Najm type | (Orphanet:163937) |
X-linked recessive ocular albinism | (Orphanet:54) |
Xp22.3 microdeletion syndrome | (Orphanet:1643) |
Zimmermann-Laband syndrome | (Orphanet:3473) |
[DEL] SENGERS SYNDROME | (OMIM:212350) |
Åland Islands eye disease | (Orphanet:178333) |