Mapping of Health Care Providers
for People with Rare 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 syndrome Anophthalmia/microphthalmia-esophageal atresia syndrome Anterior segment dysgenesis 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 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-epicanthus inversus-ptosis 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 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 intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Corneodermatoosseous syndrome Corneogoniodysgenesis Corneoiridogoniodysgenesis Cryptophthalmia Cystoid macular dystrophy Dermochondrocorneal dystrophy Developmental defect of the eye Disease predisposing to age-related macular degeneration Distal monosomy 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 Endotheliitis Epiblepharon Epicanthal fold Epithelial basement membrane dystrophy Epithelial recurrent erosion dystrophy Essential iris atrophy Euryblepharon Excretory apparatus of the lacrimal system anomaly Eyelid border anomaly Eyelid malformation Eyelids malposition disorder Familial benign flecked retina Familial congenital palsy of trochlear nerve Familial drusen Familial exudative vitreoretinopathy Familial flecked retinopathy Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement 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-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 glaucoma Hereditary hyperferritinemia-cataract syndrome Hereditary optic neuropathy Hereditary retinoblastoma Hereditary vascular retinopathy Hermansky-Pudlak syndrome with neutropenia 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 Intellectual disability-alacrima-achalasia syndrome Intermediate uveitis Iridocorneal endothelial syndrome Iridogoniodysgenesis Isolated aniridia Isolated ankyloblepharon filiforme adnatum Isolated anophthalmia-microphthalmia syndrome Isolated congenital alacrima Isolated congenital ectropion Isolated congenital megalocornea Isolated congenital sclerocornea Isolated cryptophthalmia Isolated distichiasis Isolated ectopia lentis Isolated optic nerve hypoplasia/aplasia Juvenile cataract-microcornea-renal glucosuria syndrome Juvenile glaucoma Kandori fleck retina Kein Name gefunden Kein Name gefunden Keratoconus Kinetic eyelid anomaly Knobloch syndrome Late-onset retinal degeneration Lattice corneal dystrophy type I Leber congenital amaurosis Leber hereditary optic neuropathy Leber plus disease Lens and zonula anomaly 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 Maternally-inherited progressive external ophthalmoplegia 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-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 Moebius syndrome Morning glory syndrome Muir-Torre syndrome Multifocal pattern dystrophy simulating fundus flavimaculatus Myopic macular degeneration Nanophthalmia Neovascular glaucoma Nervous system anomaly with eye involvement Neuro-ophthalmological disease Neurogenic palpebral tumor Neuromyelitis optica 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 coloboma Ocular motor apraxia, Cogan type Ocular pemphigoid 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 or related oculomotor disease Oculomotor palsy Oguchi disease Okihiro syndrome Okihiro syndrome due to 20q13 microdeletion Okihiro syndrome due to a point mutation Oligocone trichromacy Optic atrophy-intellectual disability syndrome Optic nerve edema-splenomegaly 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 Patterned dystrophy of the retinal pigment epithelium 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 glaucoma 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 cataract Rare conjunctival disease Rare disease with glaucoma as a major feature Rare disorder with ptosis Rare eye disease Rare eye disease due to a differentiation anomaly Rare genetic eye disease Rare hyperopia and astigmatism Rare inflammatory eye disease Rare isolated myopia Rare lacrimal system disease Rare palpebral disease Rare palpebral, lacrimal system and conjunctival disease Rare refraction anomaly Rare strabismus and restriction syndrome Reis-Bücklers corneal dystrophy Renal coloboma syndrome Reticular dystrophy of the retinal pigment epithelium Retinal capillary malformation Retinal degeneration-nanophthalmos-glaucoma syndrome Retinal dystrophy Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies 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 dysgenetic glaucoma 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 Stromal keratitis Subepithelial mucinous corneal dystrophy Superficial corneal dystrophy Superior limbic keratoconjunctivitis Supranuclear oculomotor palsy Sympathetic ophthalmia Syndrome with a symptomatic strabismus Syndromic aniridia Syndromic cataract Syndromic corneal dystrophy Syndromic hyperopia Syndromic keratoconus Syndromic microphthalmia Syndromic microphthalmia type 5 Syndromic oculocutaneous albinism Syndromic optic nerve hypoplasia Syndromic retinitis pigmentosa Systemic diseases with anterior uveitis Systemic diseases with panuveitis Systemic diseases with posterior uveitis Tarsal kink syndrome Telecanthus 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