Patient Information: M

Patient Information
Macrophthalmia with Microcornea and Colobomas
Macular Degeneration, Early-Onset
Macular Dystrophy with Central Cone Involvement
Macular Dystrophy, Fenestrated Type
Macular Dystrophy, North Carolina
Macular Dystrophy, Occult
Macular Dystrophy, Patterned 1
Macular Dystrophy, Patterned 2
Macular Dystrophy, Patterned 3
Macular Dystrophy, Vitelliform 1
Macular Dystrophy, Vitelliform 2
Macular Dystrophy, Vitelliform 3
Macular Dystrophy, Vitelliform 4
Macular Dystrophy, Vitelliform 5
Macular Edema, Autosomal Dominant Cystoid
Majewski Syndrome
Mandibulofacial Dysostosis with Alopecia
Manitoba Oculotrichoanal Syndrome
Mannosidosis, Alpha B
Marfan Lipodystrophy Syndrome
Marfan Syndrome
Marinesco-Sjogren Syndrome
Maroteaux-Lamy Syndrome (MPS VI)
Marshall Syndrome
McCune-Albright Syndrome
Meckel Syndrome
Meester-Loeys Syndrome
Megalocornea, Ectopia Lentis, and Spherophakia
MELAS Syndrome
Mental Retardation, AD 34
Mental Retardation, X-Linked 99, Syndromic, Female-Restricted
Microcephaly, Congenital Cataracts, and Psoriasiform Dermatitis
Microcoria, Congenital
Microcornea, Myopia, Telecanthus and Posteriorly-Rotated Ears
Microphthalmia and Anophthalmia, ALDH1A3 Associated
Microphthalmia with Coloboma, AD
Microphthalmia with Coloboma, X-Linked
Microphthalmia with Limb Anomalies
Microphthalmia with Retinitis Pigmentosa
Microphthalmia, AR
Microphthalmia, Isolated, with Cataract
Microphthalmia, Syndromic 1
Microphthalmia, Syndromic 10
Microphthalmia, Syndromic 2
Microphthalmia, Syndromic 3
Microphthalmia, Syndromic 4
Microphthalmia, Syndromic 5
Microphthalmia, Syndromic 6
Microphthalmia, Syndromic 7
Microphthalmia, Syndromic 8
Microphthalmia, Syndromic 9
Mitochondrial DNA Depletion Syndrome 1
Mitochondrial DNA Depletion Syndrome 3
Mitochondrial Short-Chain Enoyl-CoA Hydratase 1 Deficiency
Möebius Syndrome
Morquio Syndrome (MPS IVA)
Morquio Syndrome (MPS IVB)
Mowat-Wilson Syndrome
Multiple Endocrine Neoplasia, Type IIB
Multiple Mitochondrial Dysfunctions Syndrome 4
Muscular Dystrophy, Congenital, with Cataracts and Intellectual Disability
Myasthenic Syndromes, Congenital, Including AChR Deficiency
Myopia 1, X-linked, Nonsyndromal
Myopia 2, Autosomal Dominant, Nonsyndromal
Myopia 25, Autosomal Dominant, Nonsyndromic
Myopia and Deafness
Myopia, AR, with Cataracts and Vitreoretinal Degeneration
Myotonic Dystrophy 1
Myotonic Dystrophy 2