Progressive visual loss
Symptom Information:
Symptom ID: | HPO:0000529 | ||||||||||||||||||||||
Synonyms: |
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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) Progressive visual loss(HPO:0000529) MedDRA: |
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Database Frequency: | 54 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Ataxia - hypogonadism - choroidal dystrophy | (Orphanet:1180) |
BASAL LAMINAR DRUSEN | (OMIM:126700) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CLN1 disease | (Orphanet:228329) |
CLN10 disease | (Orphanet:228337) |
CLN11 disease | (Orphanet:314629) |
CLN2 disease | (Orphanet:228349) |
CLN3 disease | (Orphanet:228346) |
CLN5 disease | (Orphanet:228360) |
CLN6 disease | (Orphanet:228363) |
CLN7 disease | (Orphanet:228366) |
CLN8 disease | (Orphanet:228354) |
CLN9 disease | (Orphanet:228357) |
CONE-ROD DYSTROPHY 10 | (OMIM:610283) |
CONE-ROD DYSTROPHY 15 | (OMIM:613660) |
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT | (OMIM:122860) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Choroideremia | (Orphanet:180) |
Choroideremia - deafness - obesity | (Orphanet:1435) |
Congenital cataract, Volkmann type | (Orphanet:98983) |
Congenital neuronal ceroid lipofuscinosis | (Orphanet:168486) |
Congenital stromal corneal dystrophy | (Orphanet:101068) |
Craniodiaphyseal dysplasia | (Orphanet:1513) |
Donnai-Barrow syndrome | (Orphanet:2143) |
EPILEPSY, PROGRESSIVE MYOCLONIC, 5 | (OMIM:613832) |
Early-onset progressive neurodegeneration - blindness - ataxia - spasticity | (Orphanet:352654) |
FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM | (OMIM:264420) |
HERNS syndrome | (Orphanet:63261) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Late infantile neuronal ceroid lipofuscinosis | (Orphanet:168491) |
Lattice corneal dystrophy type I | (Orphanet:98964) |
Leber plus disease | (Orphanet:99718) |
Mohr-Tranebjaerg syndrome | (Orphanet:52368) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Osteopetrosis - hypogammaglobulinemia | (Orphanet:178389) |
Progressive cone dystrophy | (Orphanet:1871) |
RETINAL CONE DYSTROPHY 1 | (OMIM:180020) |
RETINITIS PIGMENTOSA 38 | (OMIM:613862) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Scheie syndrome | (Orphanet:93474) |
Schnyder corneal dystrophy | (Orphanet:98967) |
Sialidosis type 1 | (Orphanet:812) |
Spinocerebellar ataxia type 7 | (Orphanet:94147) |
Spondylometaphyseal dysplasia - cone-rod dystrophy | (Orphanet:85167) |
Subepithelial mucinous corneal dystrophy | (Orphanet:98959) |
Wolfram syndrome 1 | (OMIM:222300) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |
X-linked retinoschisis | (Orphanet:792) |