Eye diseases | Page 2

572 diseases found in 6 pages

C Diseases

Chromosome 5p duplication Chronic granulomatous disease Chronic progressive external ophthalmoplegia Coats disease Cockayne syndrome type I Cockayne syndrome type II Cockayne syndrome type III Cogan-Reese syndrome Cohen syndrome Coloboma of macula Coloboma of macula with type B brachydactyly Cone dystrophy Cone dystrophy X-linked with tapetal-like sheen Cone-rod dystrophy Cone-rod dystrophy 1 Cone-rod dystrophy 2 Cone-rod dystrophy 3 Cone-rod dystrophy 5 Cone-rod dystrophy 6 Cone-rod dystrophy X-linked 1 Cone-rod dystrophy X-linked 2 Cone-rod dystrophy X-linked 3 Congenital cystic eye Congenital disorders of glycosylation Congenital fibrosis of extraocular muscles Congenital microcoria Congenital myasthenic syndrome with episodic apnea Congenital primary aphakia Corneal dystrophy and perceptive deafness Corneal dystrophy Avellino type Corneal dystrophy crystalline of Schnyder Corneal dystrophy of Bowman layer type 1 Corneal dystrophy Thiel Behnke type Corneal endothelial dystrophy type 2 Corneal hypesthesia, familial Cornelia de Lange syndrome Corneodermatoosseous syndrome Cortical blindness-intellectual disability-polydactyly syndrome Cri du chat syndrome Crouzon syndrome Cystinosis

D Diseases

Deafness and myopia syndrome Dentatorubral-pallidoluysian atrophy Dermochondrocorneal dystrophy of François Dermoids of cornea Developmental prosopagnosia Dopamine beta hydroxylase deficiency Doyne honeycomb retinal dystrophy Duane syndrome Dubowitz syndrome Duchenne muscular dystrophy Dyskeratosis congenita Dyskeratosis congenita autosomal dominant Dyskeratosis congenita autosomal recessive Dyskeratosis congenita X-linked Dyssegmental dysplasia and glaucoma

E Diseases

Eales disease Early-onset anterior polar cataract Early-onset zonular cataract Ectodermal dysplasia skin fragility syndrome Ectopia lentis, isolated autosomal recessive EEC syndrome EEM syndrome Enthesitis-related juvenile idiopathic arthritis Epidermolysa bullosa simplex with muscular dystrophy Epithelial basement membrane corneal dystrophy

F Diseases

Fabry disease Familial amyloidosis, Finnish type Familial congenital palsy of trochlear nerve Familial cylindromatosis Familial dysautonomia Familial exudative vitreoretinopathy Familial LCAT deficiency Familial visceral myopathy with external ophthalmoplegia Farber's disease Fatty acid hydroxylase-associated neurodegeneration Fine-Lubinsky syndrome Fish-eye disease Focal dermal hypoplasia Fragile X syndrome Fraser syndrome Friedreich ataxia Frontofacionasal dysplasia Fuchs endothelial corneal dystrophy Fuchs heterochromic iridocyclitis Fukuyama type muscular dystrophy Fundus dystrophy, pseudoinflammatory, of Sorsby

G Diseases

Galactokinase deficiency Galactosialidosis GAPO syndrome Gardner syndrome Gaucher disease - ophthalmoplegia - cardiovascular calcification Gaucher disease type 1 Gaucher disease type 2 Gaucher disease type 3 Gillespie syndrome Glaucoma, Ectopia, Microspherophakia, Stiff joints and Short stature syndrome Glaucoma sleep apnea GM1 gangliosidosis type 1 GM1 gangliosidosis type 2

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

People Using the App

Join the RareGuru Community

To connect, share, empower and heal today.

People Using the App