Astigmatism
Symptom Information:
Symptom ID: | HPO:0000483 | |||||||||||||
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 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) |
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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) |
Ă…land Islands eye disease | (Orphanet:178333) |