Reduced visual acuity
Symptom Information:
Symptom ID: | HPO:0007663 | ||||
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 vision(HPO:0000504) Visual impairment(HPO:0000505) Visual loss(HPO:0000572) Reduced visual acuity(HPO:0007663) MedDRA: |
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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) |