Progressive visual loss

Symptom Information:

Symptom ID: HPO:0000529
Synonyms:
DECREASED VISUAL ACUITY, PROGRESSIVE [HPO:0000529]
Loss of visual acuity [HPO:0000529]
Progressive loss of vision [HPO:0000529]
Progressive vision loss [HPO:0000529]
Progressive visual acuity loss [HPO:0000529]
Progressive visual impairment [HPO:0000529]
Slowly progressive visual loss [HPO:0000529]
Visual loss, progressive [HPO:0000529]
Decreased visual acuity, progressive [OMIM:Decreased visual acuity, progressive]
Loss of visual acuity [OMIM:Loss of visual acuity]
Progressive loss of vision [OMIM:Progressive loss of vision]
Progressive visual acuity loss [OMIM:Progressive visual acuity loss]
Progressive visual loss [OMIM:Progressive visual loss]
Slowly progressive visual loss [OMIM:Slowly progressive visual loss]
Visual loss, progressive [OMIM:Visual loss, progressive]
Loss of vision, progressive [OMIM:Loss of vision, progressive]
Loss of visual acuity (late) [OMIM:Loss of visual acuity (late)]
Progressive vision loss (in males and some carrier females) [OMIM:Progressive vision loss (in males and some carrier females)]
Vision loss, progressive [OMIM:Vision loss, progressive]
Vision loss, progressive (4 to 10 years) [OMIM:Vision loss, progressive (4 to 10 years)]
Vision loss, progressive (type I) [OMIM:Vision loss, progressive (type I)]
Visual impairment, progressive [OMIM:Visual impairment, progressive]
Quality:
Cross references:
OMIM: "Decreased visual acuity, progressive" [OMIM:Decreased visual acuity, progressive]
OMIM: "Loss of visual acuity" [OMIM:Loss of visual acuity]
OMIM: "Progressive loss of vision" [OMIM:Progressive loss of vision]
OMIM: "Progressive visual acuity loss" [OMIM:Progressive visual acuity loss]
OMIM: "Progressive visual loss" [OMIM:Progressive visual loss]
OMIM: "Slowly progressive visual loss" [OMIM:Slowly progressive visual loss]
OMIM: "Visual loss, progressive" [OMIM:Visual loss, progressive]
OMIM: "Loss of vision, progressive" [OMIM:Loss of vision, progressive]
OMIM: "Loss of visual acuity (late)" [OMIM:Loss of visual acuity (late)]
OMIM: "Progressive vision loss (in males and some carrier females)" [OMIM:Progressive vision loss (in males and some carrier females)]
OMIM: "Vision loss, progressive" [OMIM:Vision loss, progressive]
OMIM: "Vision loss, progressive (4 to 10 years)" [OMIM:Vision loss, progressive (4 to 10 years)]
OMIM: "Vision loss, progressive (type I)" [OMIM:Vision loss, progressive (type I)]
OMIM: "Visual impairment, progressive" [OMIM:Visual impairment, progressive]
Is a (Direct Parents):
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)
                      Progressive visual loss(HPO:0000529)
MedDRA:
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)