Astigmatism

Symptom Information:

Symptom ID: HPO:0000483
Synonyms:
Astigmatism (disorder) [Orphanet:5660]
Astigmatism [Orphanet:5660]
Astigmatism [OMIM:Astigmatism]
Astigmatism [MedDRA:10003569]
Astigmatism, unspecified [MedDRA:10003569]
Irregular astigmatism [MedDRA:10003569]
Regular astigmatism [MedDRA:10003569]
Myopic astigmatism [MedDRA:10003569]
Hyperopic astigmatism [MedDRA:10003569]
Residual astigmatism [MedDRA:10003569]
Astigmatism (1 patient) [OMIM:Astigmatism (1 patient)]
Astigmatism (in some patients) [OMIM:Astigmatism (in some patients)]
Astigmatism (rare) [OMIM:Astigmatism (rare)]
Quality:
Cross references:
Orphanet:5660 "Astigmatism" [Orphanet:5660]
OMIM: "Astigmatism" [OMIM:Astigmatism]
OMIM: "Astigmatism (1 patient)" [OMIM:Astigmatism (1 patient)]
OMIM: "Astigmatism (in some patients)" [OMIM:Astigmatism (in some patients)]
OMIM: "Astigmatism (rare)" [OMIM:Astigmatism (rare)]
UMLS:C0004106 "Astigmatism" [HPO:0000483]
UMLS:C0004106 "Astigmatism" [Orphanet:5660]
Is a (Direct Parents):
HPO         Abnormality of refraction
HPO         Abnormality of the curvature of the cornea
MedDRA Refractive and accommodative disorders
Orphanet Abnormality of the eye
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the cornea(HPO:0000481)
                      Abnormality of the curvature of the cornea(HPO:0100691)
                         Astigmatism(HPO:0000483)
          Abnormal eye physiology(HPO:0012373)
             Abnormality of refraction(HPO:0000539)
                Astigmatism(HPO:0000483)
MedDRA:
Eye disorders(MedDRA:10015919)
    Vision disorders(MedDRA:10047518)
       Refractive and accommodative disorders(MedDRA:10038267)
          Astigmatism(HPO:0000483)
Database Frequency: 67 / 7739
Resource:

All diseases associated with this symptom:

16q24.3 microdeletion syndrome (Orphanet:261250)
2q23.1 microdeletion syndrome (Orphanet:228402)
5p13 microduplication syndrome (Orphanet:329802)
Adenylosuccinate lyase deficiency (Orphanet:46)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
Autosomal recessive Stickler syndrome (Orphanet:250984)
Axial spondylometaphyseal dysplasia (Orphanet:168549)
BARATELA-SCOTT SYNDROME (OMIM:300881)
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)
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency (Orphanet:329255)
Branchiogenic deafness syndrome (Orphanet:50815)
COFFIN-SIRIS SYNDROME (OMIM:135900)
Caudal appendage - deafness (Orphanet:1123)
Coffin-Siris syndrome (Orphanet:1465)
Cone dystrophy with supernormal rod response (Orphanet:209932)
Cornelia de Lange syndrome (Orphanet:199)
Costello syndrome (Orphanet:3071)
EDICT syndrome (Orphanet:293936)
Ermine phenotype (Orphanet:999)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis (Orphanet:31043)
Familial vascular leukoencephalopathy (Orphanet:36383)
Fanconi anemia (Orphanet:84)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Helicoid peripapillary chorioretinal degeneration (Orphanet:86813)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hirsutism - skeletal dysplasia - intellectual deficit (Orphanet:2156)
Hurler-Scheie syndrome (Orphanet:93476)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Isolated ectopia lentis (Orphanet:1885)
Joubert syndrome 9 (OMIM:612285)
KERATOCONUS 1 (OMIM:148300)
Kozlowski-Brown-Hardwick syndrome (Orphanet:2352)
Leber congenital amaurosis 10 (OMIM:611755)
Lowry-Wood syndrome (Orphanet:1824)
MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE (OMIM:248000)
MEGALOCORNEA (OMIM:309300)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Mulibrey nanism (Orphanet:2576)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Ocular albinism (Orphanet:284804)
Oculo-skeletal-renal syndrome (Orphanet:2716)
Oculocutaneous albinism (Orphanet:55)
Oculocutaneous albinism type 1 (Orphanet:352731)
Paraplegia - intellectual deficit - hyperkeratosis (Orphanet:2824)
Pilodental dysplasia - refractive errors (Orphanet:2892)
Pitt-Hopkins syndrome (Orphanet:2896)
Pontocerebellar hypoplasia type 8 (Orphanet:324569)
RETINAL DYSTROPHY AND OBESITY (OMIM:616188)
RETINOPATHY, PERICENTRAL PIGMENTARY, AUTOSOMAL RECESSIVE (OMIM:268060)
Sanjad-Sakati syndrome (Orphanet:2323)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Sinus node disease and myopia (OMIM:182190)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Stickler syndrome (Orphanet:828)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)
Usher syndrome (Orphanet:886)
Usher syndrome type 3 (Orphanet:231183)
VAN BOGAERT-HOZAY SYNDROME (OMIM:277150)
X-linked cone dysfunction syndrome with myopia (Orphanet:90001)
X-linked recessive ocular albinism (Orphanet:54)
Xeroderma pigmentosum complementation group F (Orphanet:276264)
Åland Islands eye disease (Orphanet:178333)