Zentrum für Seltene Augenerkrankungen (ZSA) am Universitätsklinikum Tübingen Assigned 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