Reduced visual acuity

Symptom Information:

Symptom ID: HPO:0007663
Synonyms:
Central visual loss [HPO:0007663]
Central visual loss [OMIM:Central visual loss]
Decreased central vision [OMIM:Decreased central vision]
Decreased central vision (later in course of disease) [OMIM:Decreased central vision (later in course of disease)]
Quality:
Cross references:
OMIM: "Central visual loss" [OMIM:Central visual loss]
OMIM: "Decreased central vision" [OMIM:Decreased central vision]
OMIM: "Decreased central vision (later in course of disease)" [OMIM:Decreased central vision (later in course of disease)]
Is a (Direct Parents):
HPO         Visual acuity test abnormality
HPO         Visual loss
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 vision(HPO:0000504)
                Visual impairment(HPO:0000505)
                   Visual loss(HPO:0000572)
                      Reduced visual acuity(HPO:0007663)
MedDRA:
Database Frequency: 100 / 7739
Resource:

All diseases associated with this symptom:

ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION (OMIM:270500)
Adult-onset foveomacular vitelliform dystrophy (Orphanet:99000)
Autosomal dominant optic atrophy and cataract (Orphanet:67036)
Autosomal dominant optic atrophy and congenital deafness (Orphanet:3212)
Autosomal dominant optic atrophy, classic type (Orphanet:98673)
Autosomal recessive optic atrophy, OPA7 type (Orphanet:227976)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Autosomal recessive spastic paraplegia type 15 (Orphanet:100996)
Autosomal recessive spastic paraplegia type 48 (Orphanet:306511)
Autosomal recessive spastic paraplegia type 55 (Orphanet:320375)
BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME (OMIM:615722)
Best vitelliform macular dystrophy (Orphanet:1243)
Blue cone monochromatism (Orphanet:16)
COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE (OMIM:216820)
CONE DYSTROPHY 4 (OMIM:613093)
CONE-ROD DYSTROPHY 12 (OMIM:612657)
CONE-ROD DYSTROPHY 13 (OMIM:608194)
CONE-ROD DYSTROPHY 20 (OMIM:615973)
CONE-ROD DYSTROPHY 5 (OMIM:600977)
CONE-ROD DYSTROPHY 6 (OMIM:601777)
CONE-ROD DYSTROPHY, X-LINKED, 1 (OMIM:304020)
CORNEAL DYSTROPHY, LATTICE TYPE IIIA (OMIM:608471)
Cherubism (Orphanet:184)
Chédiak-Higashi syndrome (Orphanet:167)
Cohen syndrome (Orphanet:193)
Combined oxidative phosphorylation defect type 15 (Orphanet:319524)
Cone rod dystrophy (Orphanet:1872)
Corneal anesthesia - deafness - intellectual deficit (Orphanet:1051)
EDICT syndrome (Orphanet:293936)
EXUDATIVE VITREORETINOPATHY 2, X-LINKED (OMIM:305390)
EXUDATIVE VITREORETINOPATHY 3 (OMIM:605750)
EXUDATIVE VITREORETINOPATHY 4 (OMIM:601813)
EXUDATIVE VITREORETINOPATHY 5 (OMIM:613310)
FOVEAL HYPOPLASIA 2 (OMIM:609218)
Familial exudative vitreoretinopathy (Orphanet:891)
Focal dermal hypoplasia (Orphanet:2092)
Gelatinous drop-like corneal dystrophy (Orphanet:98957)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
Granular corneal dystrophy type II (Orphanet:98963)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome type 7 (Orphanet:231531)
Hermansky-Pudlak syndrome with neutropenia (Orphanet:183678)
Hypotrichosis with juvenile macular degeneration (Orphanet:1573)
Isolated optic nerve hypoplasia (Orphanet:137902)
Leber congenital amaurosis 1 (OMIM:204000)
Leber congenital amaurosis 14 (OMIM:613341)
Leber congenital amaurosis 16 (OMIM:614186)
Leber congenital amaurosis 2 (OMIM:204100)
Leber congenital amaurosis 4 (OMIM:604393)
MACULAR DEGENERATION, EARLY-ONSET (OMIM:616118)
MACULAR DEGENERATION, X-LINKED ATROPHIC (OMIM:300834)
MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT (OMIM:616170)
MACULAR DYSTROPHY, VITELLIFORM, 1 (OMIM:153840)
MACULAR DYSTROPHY, VITELLIFORM, 4 (OMIM:616151)
MACULAR DYSTROPHY, VITELLIFORM, 5 (OMIM:616152)
MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES (OMIM:606772)
MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3 (OMIM:616335)
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9 (OMIM:615145)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 12 (OMIM:615249)
MYOPIA 22, AUTOSOMAL DOMINANT (OMIM:615420)
MYOPIA 23, AUTOSOMAL RECESSIVE (OMIM:615431)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Microphthalmia - retinitis pigmentosa - foveoschisis - optic disc drusen (Orphanet:251279)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
NANOPHTHALMOS 4 (OMIM:615972)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C (OMIM:613216)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E (OMIM:614565)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A (OMIM:300071)
NYSTAGMUS 1, CONGENITAL, X-LINKED (OMIM:310700)
NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT (OMIM:164100)
OPTIC ATROPHY 8 (OMIM:616289)
Ocular albinism with congenital sensorineural deafness (Orphanet:352740)
Oculocerebrorenal syndrome (Orphanet:534)
Oculocutaneous albinism type 1 (Orphanet:352731)
Oculocutaneous albinism type 2 (Orphanet:79432)
Oculocutaneous albinism type 6 (Orphanet:370097)
PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX (OMIM:260480)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Progressive retinal dystrophy due to retinol transport defect (Orphanet:352718)
Pseudoxanthoma elasticum (Orphanet:758)
RETINAL CONE DYSTROPHY 3A (OMIM:610024)
RETINAL DYSTROPHY AND OBESITY (OMIM:616188)
RETINITIS PIGMENTOSA 50 (OMIM:613194)
RETINITIS PIGMENTOSA 56 (OMIM:613581)
RETINITIS PIGMENTOSA 60 (OMIM:613983)
RETINITIS PIGMENTOSA 66 (OMIM:615233)
RETINITIS PIGMENTOSA WITH OR WITHOUT SITUS INVERSUS (OMIM:615434)
RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION (OMIM:268050)
RFT1-CDG (Orphanet:244310)
RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA (OMIM:610319)
Retinal macular dystrophy type 2 (Orphanet:319640)
Retinopathy, Burgess-Black type (Orphanet:139455)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
STARGARDT DISEASE 3 (OMIM:600110)
STARGARDT DISEASE 4 (OMIM:603786)
Senior-Loken syndrome 6 (OMIM:610189)
Senior-Loken syndrome 8 (OMIM:616307)
Spinocerebellar ataxia type 25 (Orphanet:101111)
Usher syndrome type 3 (Orphanet:231183)
[DEL] PSEUDOXANTHOMA ELASTICUM (OMIM:264800)