SE-ATLAS

Endotheliale Hornhautdystrophie Fuchs Zapfendystrophie mit supernormalen Stäbchen-B-Wellen Amaurosis congenita Leber Panuveitis Retinale Vaskulopathie mit zerebraler Leukoenzephalopathie und systemischen Manifestationen Netzhautdystrophie Typ Bottnien Progressive Retinadystrophie durch Retinol-Transportdefekt Chorioretinale Degeneration, helikoid-peripapilläre X-chromosomale Intelligenzminderung-Spastizität der Extremitäten-Netzhautdystrophie-Diabetes insipidus-Syndrom Mikrokornea-myopische chorioretinale Atrophie-Telekanthus-Syndrom MORM-Syndrom Retinitis pigmentosa, syndromale Netzhautdystrophie, hereditäre, sonstige Atrophie, bifokale chorioretinale progressive Netzhautkrankheit, isolierte, hereditäre Formen Oguchi disease Brachydactyly-short stature-retinitis pigmentosa syndrome Uveitis Pigmented paravenous retinochoroidal atrophy Åland Islands eye disease Aceruloplasminemia Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies Autosomal recessive bestrophinopathy Familial benign flecked retina Revesz syndrome Severe early-childhood-onset retinal dystrophy Retinitis pigmentosa Martinique crinkled retinal pigment epitheliopathy Retinal degeneration-nanophthalmos-glaucoma syndrome Anterior uveitis Posterior uveitis X-linked retinal dysplasia Ectopia lentis-chorioretinal dystrophy-myopia syndrome Genetic macular dystrophy Intermediate uveitis Oligocone trichromacy Syndromic inherited retinal disorder Gyrate atrophy of choroid and retina Inherited retinal disorder MRCS syndrome Autosomal recessive chorioretinopathy-microcephaly syndrome Microcephaly-lymphedema-chorioretinopathy syndrome Late-onset retinal degeneration Amaurosis-hypertrichosis syndrome Infantile cerebellar-retinal degeneration