Eye diseases | Page 4

572 diseases found in 6 pages

M Diseases

Melnick-Needles syndrome Menkes disease Methylmalonic acidemia with homocystinuria type cblC Mevalonic aciduria Microcephaly microcornea syndrome Seemanova type Microcornea corectopia macular hypoplasia Microcornea posterior megalolenticonus persistent fetal vasculature coloboma Microphthalmia syndromic 10 Microphthalmia syndromic 4 Microphthalmia syndromic 5 Microphthalmia syndromic 6 Microphthalmia syndromic 8 Microphthalmia syndromic 9 Microphthalmia with linear skin defects syndrome Microspherophakia with hernia Micro syndrome Microtia eye coloboma and imperforation of the nasolacrimal duct Miller syndrome Milroy disease Mitochondrial DNA-associated Leigh syndrome Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes Mitochondrial Membrane Protein-Associated Neurodegeneration Mitochondrial neurogastrointestinal encephalopathy syndrome Moebius syndrome Mohr-Tranebjaerg syndrome Molybdenum cofactor deficiency Morning glory syndrome Mousa Al din Al Nassar syndrome Mucolipidosis type 4 Mucopolysaccharidosis type III Mucopolysaccharidosis type IIIA Mucopolysaccharidosis type IIIB Mucopolysaccharidosis type IIIC Mucopolysaccharidosis type IIID Mucopolysaccharidosis type IV Mucopolysaccharidosis type IVA Mucopolysaccharidosis type VII Muir-Torre syndrome Multiple familial trichoepithelioma Multiple familial trichoepithelioma 1 Multiple familial trichoepithelioma 2 Muscle eye brain disease Myoclonic epilepsy with ragged red fibers Myotonic dystrophy type 1 Myotonic dystrophy type 2

N Diseases

Nager acrofacial dysostosis Nail-patella syndrome Nance-Horan syndrome Nathalie syndrome Neonatal adrenoleukodystrophy Neonatal Onset Multisystem Inflammatory disease Neonatal progeroid syndrome Netherton syndrome Neurofibromatosis type 2 Neuromyelitis optica Neuronal ceroid lipofuscinosis Neuronal ceroid lipofuscinosis 10 Neuronal ceroid lipofuscinosis 5 Neuronal ceroid lipofuscinosis 6 Neuronal ceroid lipofuscinosis 7 Neuropathy ataxia retinitis pigmentosa syndrome Nevoid basal cell carcinoma syndrome Niemann-Pick disease type A Niemann-Pick disease type C1 Niemann-Pick disease type C2 Noonan syndrome Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Norrie disease North Carolina macular dystrophy Nystagmus 1, congenital, X- linked Nystagmus 2, congenital, autosomal dominant

O Diseases

Ocular albinism type 1 Ocular neuromyotonia Oculoauriculofrontonasal syndrome Oculocerebral syndrome with hypopigmentation Oculocutaneous albinism type 1 Oculocutaneous albinism type 1B Oculocutaneous albinism type 2 Oculocutaneous albinism type 3 Oculodentodigital dysplasia Oculofaciocardiodental syndrome Oculomotor apraxia Cogan type Oculopharyngeal muscular dystrophy Oculopharyngodistal myopathy O Donnell Pappas syndrome Oguchi disease OPA3 defect Opsoclonus-myoclonus syndrome Optic atrophy 1 Optic atrophy 2 Optic atrophy 5 Optic atrophy 6 Optic neuritis Orbital varix Osteopetrosis autosomal dominant type 2

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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