Mapping of Health Care Providers
for People with Rare Diseases

In the following you will find the diseases that are treated in this facility:
3-methylglutaconic aciduria type 3 Abnormal eye movements Aceruloplasminemia Acute endophthalmitis Adult-onset foveomacular vitelliform dystrophy Alström syndrome Amaurosis-hypertrichosis syndrome Aniridia Anterior uveitis Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome Ataxia-oculomotor apraxia type 1 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 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 Best vitelliform macular dystrophy Bietti crystalline dystrophy Birdshot chorioretinopathy Bothnia retinal dystrophy Butterfly-shaped pigment dystrophy Central areolar choroidal dystrophy Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Cerebroretinal vasculopathy Chandler syndrome Childhood-onset autosomal recessive myopathy with external ophthalmoplegia Choroideremia Chronic endophthalmitis Coats disease Cogan syndrome Cogan-Reese syndrome Coloboma of macula Coloboma of macula-brachydactyly type B syndrome Colobomatous and areolar dystrophy Cone dystrophy with supernormal rod response Cone rod dystrophy Congenital ectropion uveae Congenital glaucoma Congenital microcoria Congenital stationary night blindness Congenital trigeminal anesthesia Congenital trochlear nerve palsy Corneogoniodysgenesis Corneoiridogoniodysgenesis Cystoid macular dystrophy Distal monosomy 6p Duane retraction syndrome EEM syndrome Early-onset X-linked optic atrophy Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome Ectopia lentis-chorioretinal dystrophy-myopia syndrome Endophthalmitis Endotheliitis Essential iris atrophy Familial benign flecked retina Familial congenital palsy of trochlear nerve Familial drusen Familial flecked retinopathy Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement Fatty acid hydroxylase-associated neurodegeneration Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome Foveal hypoplasia-presenile cataract syndrome Fuchs heterochromic iridocyclitis Fundus albipunctatus Fundus pulverulentus GAPO syndrome Genetic macular dystrophy Glaucoma associated with neural crest cell migration anomaly Glaucoma secondary to spherophakia/ectopia lentis and megalocornea Goldmann-Favre syndrome Goniodysgenesis Gonococcal conjunctivitis Gyrate atrophy of choroid and retina HERNS syndrome Helicoid peripapillary chorioretinal degeneration Hereditary glaucoma Hereditary optic neuropathy Hereditary vascular retinopathy Hermansky-Pudlak syndrome with neutropenia Horizontal gaze palsy with progressive scoliosis Hypotrichosis with juvenile macular degeneration Idiopathic anterior uveitis Idiopathic panuveitis Idiopathic posterior uveitis Idiopathic uveal effusion syndrome Infectious anterior uveitis Infectious epithelial keratitis Infectious panuveitis Infectious posterior uveitis Intermediate uveitis Iridocorneal endothelial syndrome Iridogoniodysgenesis Isolated congenital megalocornea Isolated congenital sclerocornea Isolated optic nerve hypoplasia/aplasia Juvenile glaucoma Kandori fleck retina Kein Name gefunden Kein Name gefunden Late-onset retinal degeneration Leber congenital amaurosis Leber hereditary optic neuropathy Leber plus disease Ligneous conjunctivitis MORM syndrome MRCS syndrome Macular coloboma-cleft palate-hallux valgus syndrome Maternally-inherited progressive external ophthalmoplegia Microcornea-myopic chorioretinal atrophy-telecanthus syndrome Moebius syndrome Morning glory syndrome Multifocal pattern dystrophy simulating fundus flavimaculatus Nervous system anomaly with eye involvement Neuro-ophthalmological disease Neurotrophic keratopathy Non-infectious anterior uveitis Non-infectious posterior uveitis North Carolina macular dystrophy Nuclear oculomotor paralysis Occult macular dystrophy Ocular motor apraxia, Cogan type Ocular pemphigoid 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 Panuveitis Paraneoplastic uveitis Patterned dystrophy of the retinal pigment epithelium Peters anomaly Peters plus syndrome Phacoanaphylactic uveitis Pigmented paravenous retinochoroidal atrophy Polymicrogyria with optic nerve hypoplasia Posterior polymorphous corneal dystrophy Posterior uveitis Primary ciliary dyskinesia-retinitis pigmentosa syndrome Primary glaucoma Progressive bifocal chorioretinal atrophy Progressive cone dystrophy Progressive retinal dystrophy due to retinol transport defect Rare eye disease Rare inflammatory eye disease Rare strabismus and restriction syndrome Reticular dystrophy of the retinal pigment epithelium 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 Revesz syndrome Rieger anomaly Secondary dysgenetic glaucoma Secondary glaucoma due to a proliferation and differentiation anomaly Septo-optic dysplasia spectrum Serpiginous choroiditis Severe early-childhood-onset retinal dystrophy Sorsby pseudoinflammatory fundus dystrophy 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 keratitis Superior limbic keratoconjunctivitis Supranuclear oculomotor palsy Sympathetic ophthalmia Syndrome with a symptomatic strabismus Syndromic optic nerve hypoplasia Syndromic retinitis pigmentosa Systemic diseases with anterior uveitis Systemic diseases with panuveitis Systemic diseases with posterior uveitis Tolosa-Hunt syndrome Unclassified familial retinal dystrophy Unclassified primitive or secondary maculopathy Usher syndrome Usher syndrome type 1 Usher syndrome type 2 Usher syndrome type 3 Uveitis Vernal keratoconjunctivitis Vogt-Koyanagi-Harada disease WAGR syndrome X-linked retinal dysplasia X-linked retinoschisis Åland Islands eye disease