Blinden- und Sehbehindertenverein Westfalen e.V. (BSVW) Assigned diseases:
In the following you will find the diseases that this support group organisation focuses on:
3-methylglutaconic aciduria type 3
AGel amyloidosis
Ablepharon macrostomia syndrome
Abnormal eye movements
Aceruloplasminemia
Achromatopsia
Acute annular outer retinopathy
Acute endophthalmitis
Acute zonal occult outer retinopathy
Adult-onset foveomacular vitelliform dystrophy
Alström syndrome
Amaurosis-hypertrichosis syndrome
Aniridia
Aniridia-absent patella syndrome
Aniridia-cerebellar ataxia-intellectual disability syndrome
Aniridia-intellectual disability syndrome
Aniridia-ptosis-intellectual disability-familial obesity syndrome
Aniridia-renal agenesis-psychomotor retardation syndrome
Anophthalmia/microphthalmia-esophageal atresia syndrome
Anterior segment developmental anomaly
Anterior segment developmental anomaly without extraocular manifestations
Anterior uveitis
Aplasia of lacrimal and salivary glands
Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome
Ataxia-oculomotor apraxia type 1
Atopic keratoconjunctivitis
Autosomal dominant keratitis
Autosomal dominant neovascular inflammatory vitreoretinopathy
Autosomal dominant optic atrophy
Autosomal dominant optic atrophy and cataract
Autosomal dominant optic atrophy and peripheral neuropathy
Autosomal dominant optic atrophy plus syndrome
Autosomal dominant optic atrophy, classic form
Autosomal dominant rhegmatogenous retinal detachment
Autosomal dominant vitreoretinochoroidopathy
Autosomal recessive Stickler syndrome
Autosomal recessive bestrophinopathy
Autosomal recessive isolated optic atrophy
Autosomal recessive optic atrophy, OPA7 type
Axenfeld anomaly
Axenfeld-Rieger syndrome
Bardet-Biedl syndrome
Behr syndrome
Benign concentric annular macular dystrophy
Benign tumor of palpebral epidermis
Best vitelliform macular dystrophy
Bietti crystalline dystrophy
Bilateral acute depigmentation of the iris
Birdshot chorioretinopathy
Blepharo-cheilo-odontic syndrome
Blepharophimosis-ptosis-epicanthus inversus syndrome
Blepharoptosis-myopia-ectopia lentis syndrome
Blindness-scoliosis-arachnodactyly syndrome
Blue cone monochromatism
Bothnia retinal dystrophy
Bradyopsia
Bulbar conjunctival dermoid or conjunctival dermolipoma
Butterfly-shaped pigment dystrophy
Cancer-associated retinopathy
Canthal anomaly
Cataract-glaucoma syndrome
Cataract-microcornea syndrome
Central areolar choroidal dystrophy
Central cloudy dystrophy of François
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
Cerebroretinal vasculopathy
Cerulean cataract
Chandler syndrome
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia
Chondroectodermal dysplasia with night blindness
Choroideremia
Chronic endophthalmitis
Coats disease
Coats plus syndrome
Cogan syndrome
Cogan-Reese syndrome
Coloboma of choroid and retina
Coloboma of eye lens
Coloboma of eyelid
Coloboma of iris
Coloboma of macula
Coloboma of macula-brachydactyly type B syndrome
Coloboma of optic disc
Colobomatous and areolar dystrophy
Colobomatous microphthalmia
Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome
Color-vision disease
Cone dystrophy with supernormal rod response
Cone rod dystrophy
Congenital Horner syndrome
Congenital alacrima
Congenital cataract microcornea with corneal opacity
Congenital cornea plana
Congenital ectropion
Congenital ectropion uveae
Congenital entropion
Congenital eyelid retraction
Congenital glaucoma
Congenital hereditary endothelial dystrophy type I
Congenital hereditary endothelial dystrophy type II
Congenital malformation of the eye with glaucoma as a major feature
Congenital malformation of the eyelid
Congenital microcoria
Congenital primary aphakia
Congenital retinal arteriovenous communication
Congenital stationary night blindness
Congenital stromal corneal dystrophy
Congenital trigeminal anesthesia
Congenital trochlear nerve palsy
Congenital upper palpebral retraction
Congenital vitreoretinal dysplasia
Conjunctival hemangioma or hemolymphangioma
Conjunctival lymphangiectasia
Conjunctival telangiectasia
Conjunctival tumor
Conjunctival vascular anomaly
Coralliform cataract
Corneal dystrophy
Corneal dystrophy-perceptive deafness syndrome
Corneal endotheliitis
Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome
Corneodermatoosseous syndrome
Corneodysgenesis
Corneoiridogoniodysgenesis
Cryptophthalmia
Cystoid macular dystrophy
Dermochondrocorneal dystrophy
Developmental defect of the eye
Disease predisposing to age-related macular degeneration
Distal deletion 6p
Duane retraction syndrome
Dyssegmental dysplasia-glaucoma syndrome
EDICT syndrome
EEM syndrome
Eales disease
Early-onset X-linked optic atrophy
Early-onset anterior polar cataract
Early-onset non-syndromic cataract
Early-onset nuclear cataract
Early-onset partial cataract
Early-onset posterior polar cataract
Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome
Early-onset sutural cataract
Early-onset zonular cataract
Ectopia lentis-chorioretinal dystrophy-myopia syndrome
Endophthalmitis
Epiblepharon
Epicanthal fold
Epithelial basement membrane dystrophy
Epithelial recurrent erosion dystrophy
Essential iris atrophy
Essential strabismus
Euryblepharon
Eyelid border anomaly
Familial benign flecked retina
Familial congenital palsy of trochlear nerve
Familial drusen
Familial exudative vitreoretinopathy
Familial flecked retinopathy
Familial pterygium of the conjunctiva
Familial retinal arterial macroaneurysm
Fatty acid hydroxylase-associated neurodegeneration
Fleck corneal dystrophy
Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome
Fuchs endothelial corneal dystrophy
Fuchs heterochromic iridocyclitis
Fundus albipunctatus
Fundus pulverulentus
GAPO syndrome
Gardner syndrome
Gelatinous drop-like corneal dystrophy
Genetic macular dystrophy
Genetic vitreous-retinal disease
Glaucoma associated with neural crest cell migration anomaly
Glaucoma secondary to spherophakia/ectopia lentis and megalocornea
Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome
Goldmann-Favre syndrome
Goniodysgenesis
Gonococcal conjunctivitis
Granular corneal dystrophy type I
Granular corneal dystrophy type II
Grayson-Wilbrandt corneal dystrophy
Gyrate atrophy of choroid and retina
HERNS syndrome
Helicoid peripapillary chorioretinal degeneration
Hereditary benign intraepithelial dyskeratosis
Hereditary hyperferritinemia-cataract syndrome
Hereditary optic neuropathy
Hereditary retinoblastoma
Hereditary vascular retinopathy
Hermansky-Pudlak syndrome due to AP-3 deficiency
Herpes simplex virus stromal keratitis
High myopia-sensorineural deafness syndrome
Horizontal gaze palsy with progressive scoliosis
Hypomyelination-congenital cataract syndrome
Hypotrichosis with juvenile macular degeneration
IRVAN syndrome
Idiopathic anterior uveitis
Idiopathic linear interstitial keratitis
Idiopathic macular telangiectasia type 1
Idiopathic macular telangiectasia type 3
Idiopathic panuveitis
Idiopathic posterior uveitis
Idiopathic uveal effusion syndrome
Infectious anterior uveitis
Infectious epithelial keratitis
Infectious panuveitis
Infectious posterior uveitis
Inherited retinal disorder
Intellectual disability-alacrima-achalasia syndrome
Intermediate uveitis
Iridocorneal endothelial syndrome
Isolated aniridia
Isolated ankyloblepharon filiforme adnatum
Isolated congenital alacrima
Isolated congenital ectropion
Isolated congenital megalocornea
Isolated congenital sclerocornea
Isolated cryptophthalmia
Isolated distichiasis
Isolated ectopia lentis
Isolated microphthalmia-anophthalmia-coloboma
Isolated optic nerve hypoplasia/aplasia
Juvenile cataract-microcornea-renal glucosuria syndrome
Juvenile glaucoma
Kandori fleck retina
Keratoconus
Kinetic eyelid anomaly
Knobloch syndrome
Lacrimal drainage system anomaly
Late-onset retinal degeneration
Lattice corneal dystrophy type I
Leber congenital amaurosis
Leber hereditary optic neuropathy
Leber plus disease
Lens position anomaly
Lens shape anomaly
Lens size anomaly
Ligneous conjunctivitis
Lisch epithelial corneal dystrophy
MMEP syndrome
MORM syndrome
MRCS syndrome
Macular coloboma-cleft palate-hallux valgus syndrome
Macular corneal dystrophy
Major induction processes eye anomaly
Malignant tumor of palpebral epidermis
Matthew-Wood syndrome
Meesmann corneal dystrophy
Mesenchymatous palpebral tumor
Micro syndrome
Microblepharon-ablephara syndrome
Microcornea-corectopia-macular hypoplasia syndrome
Microcornea-glaucoma-absent frontal sinuses syndrome
Microcornea-myopic chorioretinal atrophy-telecanthus syndrome
Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome
Microphthalmia with brain and digit anomalies
Microphthalmia with linear skin defects syndrome
Microphthalmia, Lenz type
Microphthalmia-ankyloblepharon-intellectual disability syndrome
Microphthalmia-anophthalmia-coloboma
Microphthalmia-brain atrophy syndrome
Microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome
Microspherophakia-metaphyseal dysplasia syndrome
Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome
Minimal pigment oculocutaneous albinism type 1
Mitochondrial DNA-related progressive external ophthalmoplegia
Moebius syndrome
Morning glory disc anomaly
Muir-Torre syndrome
Multifocal pattern dystrophy simulating fundus flavimaculatus
Myopic macular degeneration
Nanophthalmos
Neovascular glaucoma
Nervous system anomaly with eye involvement
Neuro-ophthalmological disease
Neurogenic palpebral tumor
Neuromyelitis optica spectrum disorder
Neurotrophic keratopathy
Non-hereditary retinoblastoma
Non-infectious anterior uveitis
Non-infectious posterior uveitis
Norrie disease
North Carolina macular dystrophy
Nuclear oculomotor paralysis
Occult macular dystrophy
Ocular albinism
Ocular albinism with congenital sensorineural deafness
Ocular albinism with late-onset sensorineural deafness
Ocular cicatricial pemphigoid
Ocular coloboma
Ocular motor apraxia, Cogan type
Oculoauricular syndrome, Schorderet type
Oculocutaneous albinism
Oculocutaneous albinism type 1
Oculocutaneous albinism type 1A
Oculocutaneous albinism type 1B
Oculocutaneous albinism type 2
Oculocutaneous albinism type 3
Oculocutaneous albinism type 4
Oculocutaneous albinism type 5
Oculocutaneous albinism type 6
Oculocutaneous albinism type 7
Oculocutaneous or ocular albinism
Oculofaciocardiodental syndrome
Oculomotor apraxia
Oguchi disease
Okihiro syndrome
Okihiro syndrome due to 20q13 microdeletion
Okihiro syndrome due to a point mutation
Oligocone trichromacy
Optic atrophy-intellectual disability syndrome
PEHO syndrome
Palpebral epidermal tumor
Palpebral lentiginosis
Palpebral nevus
Palpebral piliary tumor
Palpebral sebaceous gland tumor
Palpebral tumor
Palpebral tumor with a vascular malformation
Panuveitis
Paraneoplastic uveitis
Pattern dystrophy
Pediatric-onset glaucoma of genetic origin
Pellucid marginal degeneration
Persistent hyperplastic primary vitreous
Persistent placoid maculopathy
Peters anomaly
Peters anomaly-cataract syndrome
Peters plus syndrome
Phacoanaphylactic uveitis
Pigmentation disorder with eye involvement
Pigmentation disorder with eye involvement, excluding albinism
Pigmented conjunctival lesion
Pigmented palpebral tumor
Pigmented paravenous retinochoroidal atrophy
Polymicrogyria with optic nerve hypoplasia
Posterior amorphous corneal dystrophy
Posterior corneal dystrophy
Posterior polymorphous corneal dystrophy
Posterior uveitis
Pre-Descemet corneal dystrophy
Precancerous lesion of palpebral epidermis
Primary early-onset glaucoma
Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement
Progressive bifocal chorioretinal atrophy
Progressive cone dystrophy
Progressive retinal dystrophy due to retinol transport defect
Ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome
Pulverulent cataract
Rare acquired eye disease
Rare disease with glaucoma as a major feature
Rare disorder of the lacrimal apparatus
Rare disorder with conjunctival involvement as a major feature
Rare disorder with lens opacification
Rare disorder with ptosis
Rare disorder with strabismus
Rare eye disease due to a differentiation anomaly
Rare eyelid malposition disorder
Rare genetic eye disease
Rare hyperopia and astigmatism
Rare inflammatory eye disease
Rare isolated myopia
Rare lens disease
Rare oculomotor nerve disorder
Rare ophthalmic disorder
Rare palpebral disorder
Rare palpebral, lacrimal system and conjunctival disease
Rare refraction anomaly
Reis-Bücklers corneal dystrophy
Renal coloboma syndrome
Reticular dystrophy of the retinal pigment epithelium
Retinal capillary malformation
Retinal degeneration-nanophthalmos-glaucoma syndrome
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
Retinal dystrophy-optic nerve edema-splenomegaly-anhidrosis-migraine headache syndrome
Retinal macular dystrophy type 2
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
Retinitis pigmentosa
Retinitis punctata albescens
Retinoblastoma
Retinopathy of prematurity
Revesz syndrome
Rieger anomaly
SRD5A3-CDG
Schnyder corneal dystrophy
Secondary entropion
Secondary glaucoma due to a proliferation and differentiation anomaly
Secretory apparatus of the lacrimal system anomaly
Septo-optic dysplasia spectrum
Serpiginous choroiditis
Severe early-childhood-onset retinal dystrophy
Snowflake vitreoretinal degeneration
Sorsby pseudoinflammatory fundus dystrophy
Spasmus nutans
Spastic ataxia-corneal dystrophy syndrome
Spinocerebellar ataxia with oculomotor anomaly
Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly
Stargardt disease
Stickler syndrome
Stickler syndrome type 1
Stickler syndrome type 2
Stromal corneal dystrophy
Subepithelial mucinous corneal dystrophy
Superficial corneal dystrophy
Superior limbic keratoconjunctivitis
Supranuclear eye movement disorder
Sympathetic ophthalmia
Syndromic aniridia
Syndromic cataract
Syndromic corneal dystrophy
Syndromic disorder with strabismus
Syndromic hyperopia
Syndromic keratoconus
Syndromic microphthalmia type 5
Syndromic microphthalmia-anophthalmia-coloboma
Syndromic oculocutaneous albinism
Syndromic optic nerve hypoplasia
Syndromic rod-cone dystrophy
Syndromic telecanthus
Systemic diseases with anterior uveitis
Systemic diseases with panuveitis
Systemic diseases with posterior uveitis
Tarsal kink syndrome
Temperature-sensitive oculocutaneous albinism type 1
Thiel-Behnke corneal dystrophy
Tolosa-Hunt syndrome
Total early-onset cataract
Toxic maculopathy due to antimalarial drugs
Triple A syndrome
Tritanopia
Unclassified familial retinal dystrophy
Unclassified primitive or secondary maculopathy
Usher syndrome
Usher syndrome type 1
Usher syndrome type 2
Usher syndrome type 3
Uveitis
Vasoproliferative tumor of the retina
Vernal keratoconjunctivitis
Vitreoretinal degeneration
Vitreoretinopathy
Vogt-Koyanagi-Harada disease
WAGR syndrome
Wagner disease
X-linked cone dysfunction syndrome with myopia
X-linked corneal dermoid
X-linked endothelial corneal dystrophy
X-linked recessive ocular albinism
X-linked reticulate pigmentary disorder
X-linked retinal dysplasia
X-linked retinoschisis
Åland Islands eye disease