Eye diseases | Page 1

572 diseases found in 6 pages

A Diseases

Abetalipoproteinemia Ablepharon macrostomia syndrome Aceruloplasminemia Achromatopsia 2 Achromatopsia 3 Acute intermittent porphyria Acute posterior multifocal placoid pigment epitheliopathy Acute zonal occult outer retinopathy Adult-onset vitelliform macular dystrophy ADULT syndrome Aicardi-Goutieres syndrome Aicardi syndrome Aland island eye disease Albinism ocular late onset sensorineural deafness Alexander disease Alkaptonuria Alpha-mannosidosis Alport syndrome Alström syndrome Ambras syndrome Amyloidosis corneal Aniridia Aniridia absent patella Aniridia renal agenesis psychomotor retardation Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Ankyloblepharon filiforme imperforate anus Anterior ischemic optic neuropathy Anterior segment dysgenesis Anterior uveitis Apert syndrome Aromatic L-amino acid decarboxylase deficiency Arthrogryposis renal dysfunction cholestasis syndrome Ataxia telangiectasia Ataxia with oculomotor apraxia type 1 Ataxia with Oculomotor Apraxia Type 2 Ataxia with oculomotor apraxia type 4 Ataxia with vitamin E deficiency Ausems Wittebol-Post Hennekam syndrome Autosomal dominant leukodystrophy with autonomic disease Autosomal dominant optic atrophy and cataract Autosomal dominant optic atrophy plus syndrome Autosomal dominant vitreoretinochoroidopathy Autosomal recessive Alport syndrome Autosomal recessive bestrophinopathy Autosomal recessive primary microcephaly Axenfeld-Rieger syndrome Ayazi syndrome

B Diseases

Barber Say syndrome Bardet-Biedl syndrome Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 10 Bardet-Biedl syndrome 11 Bardet-Biedl syndrome 12 Bardet-Biedl syndrome 2 Barth syndrome Bazex-Dupre-Christol syndrome Behçet disease Behr syndrome Best vitelliform macular dystrophy Bietti crystalline corneoretinal dystrophy Birdshot chorioretinopathy Blau syndrome Blepharo-cheilo-odontic syndrome Blepharophimosis with ptosis, syndactyly, and short stature Blepharoptosis myopia ectopia lentis Bloom syndrome Blue cone monochromatism Borjeson-Forssman-Lehmann syndrome Bradyopsia Brittle cornea syndrome Brown syndrome

C Diseases

CADASIL Carney complex Cataract congenital Volkmann type Cataract Hutterite type Cataract microcornea syndrome Cataract, posterior polar, 1 Cataract, posterior polar, 3 Cataract, posterior polar, 4 Cataract, posterior polar, 5 Cataract, total congenital Cat eye syndrome Centronuclear myopathy Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Cerebro-oculo-facio-skeletal syndrome Cerebrotendinous xanthomatosis Cerulean cataract Chanarin-Dorfman syndrome Chandler's syndrome CHARGE syndrome Charles Bonnet syndrome Char syndrome Chediak-Higashi syndrome Chorioretinitis Choroidal dystrophy central areolar Choroideremia Chromosome 17q11.2 deletion syndrome Chromosome 18p deletion Chromosome 21q deletion Chromosome 2q24 microdeletion syndrome

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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