Myopia

Symptom Information:

Symptom ID: HPO:0000545
Synonyms:
Myopia (disorder) [Orphanet:5630]
Myopia [Orphanet:5630]
Myopia [OMIM:Myopia]
Myopia [MedDRA:10028651]
Myopia transient [MedDRA:10028651]
Short sightedness [MedDRA:10028651]
Short-sighted [MedDRA:10028651]
Myopia aggravated [MedDRA:10028651]
Nearsighted [MedDRA:10028651]
Myopia (1/4 patients) [OMIM:Myopia (1/4 patients)]
Myopia (in 1 patient) [OMIM:Myopia (in 1 patient)]
Myopia (in 2 of 3 siblings) [OMIM:Myopia (in 2 of 3 siblings)]
Myopia (in 2 of 5 patients) [OMIM:Myopia (in 2 of 5 patients)]
Myopia (in most patients) [OMIM:Myopia (in most patients)]
Myopia (in some patients) [OMIM:Myopia (in some patients)]
Myopia (less common) [OMIM:Myopia (less common)]
Myopia (onset before 6 years) [OMIM:Myopia (onset before 6 years)]
Myopia (onset in first decade) [OMIM:Myopia (onset in first decade)]
Myopia (onset in teens) [OMIM:Myopia (onset in teens)]
Myopia (reported in 1 patient) [OMIM:Myopia (reported in 1 patient)]
Quality:
Cross references:
Orphanet:5630 "Myopia" [Orphanet:5630]
OMIM: "Myopia" [OMIM:Myopia]
OMIM: "Myopia (1/4 patients)" [OMIM:Myopia (1/4 patients)]
OMIM: "Myopia (in 1 patient)" [OMIM:Myopia (in 1 patient)]
OMIM: "Myopia (in 2 of 3 siblings)" [OMIM:Myopia (in 2 of 3 siblings)]
OMIM: "Myopia (in 2 of 5 patients)" [OMIM:Myopia (in 2 of 5 patients)]
OMIM: "Myopia (in most patients)" [OMIM:Myopia (in most patients)]
OMIM: "Myopia (in some patients)" [OMIM:Myopia (in some patients)]
OMIM: "Myopia (less common)" [OMIM:Myopia (less common)]
OMIM: "Myopia (onset before 6 years)" [OMIM:Myopia (onset before 6 years)]
OMIM: "Myopia (onset in first decade)" [OMIM:Myopia (onset in first decade)]
OMIM: "Myopia (onset in teens)" [OMIM:Myopia (onset in teens)]
OMIM: "Myopia (reported in 1 patient)" [OMIM:Myopia (reported in 1 patient)]
UMLS:C0027092 "Myopia" [HPO:0000545]
UMLS:C0027092 "Myopia" [Orphanet:5630]
Is a (Direct Parents):
Orphanet Abnormality of the eye
MedDRA Refractive and accommodative disorders
HPO         Abnormality of refraction
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)
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)