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Table 4: List of Rare Diseases and Related Terms as per US ...

Table 4: List of Rare Diseases and Related Terms as per US ...

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4016 Multiple epiphyseal dyspl<strong>as</strong>ia 3<br />

4017 Multiple epiphyseal dyspl<strong>as</strong>ia 4<br />

4018 Multiple epiphyseal dyspl<strong>as</strong>ia 5<br />

4019 Multiple familial trichoepithelioma<br />

4020 Multiple familial trichoepithelioma 1<br />

4021 Multiple familial trichoepithelioma 2<br />

4022 Multiple fibr<strong>of</strong>olliculoma familial<br />

4023 Multiple joint dislocations metaphyseal dyspl<strong>as</strong>ia<br />

4024 Multiple myeloma<br />

4025 Multiple pterygium syndrome Aslan type<br />

4026 Multiple pterygium syndrome Escobar type<br />

4027 Multiple pterygium syndrome lethal type<br />

4028 Multiple pterygium syndrome X-linked<br />

4029 Multiple respiratory chain enzyme deficiencies<br />

4030 Multiple self healing squamous epithelioma<br />

4031 Multiple sulfat<strong>as</strong>e deficiency<br />

4032 Multiple synostoses syndrome 1<br />

4033 Multiple synostoses syndrome 2<br />

4034 Multiple system atrophy<br />

4035 Multiple system atrophy (MSA) with orthostatic hypotension<br />

4036 Multiple vertebral anomalies unusual facies<br />

4037 Mumps<br />

4038 Munchausen by proxy syndrome<br />

4039 Mungan syndrome<br />

4040 MURCS <strong>as</strong>sociation<br />

4041 Muscle eye brain dise<strong>as</strong>e<br />

4042 Muscular atrophy ataxia retinitis pigmentosa <strong>and</strong> diabetes mellitus<br />

4043 Muscular dystrophy<br />

4044 Muscular Dystrophy - Late Onset<br />

4045 Muscular dystrophy limb girdle type 2A, Erb type<br />

4046 Muscular dystrophy white matter spongiosis<br />

4047 Muscular dystrophy, congenital, infantile with cataract <strong>and</strong><br />

hypogonadism<br />

4048 Muscular dystrophy, congenital, megaconial type<br />

4049 Muscular dystrophy, congenital, merosin-positive<br />

4050 Muscular fibrosis multifocal obstructed vessels<br />

4051 Muscular phosphoryl<strong>as</strong>e kin<strong>as</strong>e deficiency<br />

4052 Mutagen sensitivity<br />

4053 Mutiple parosteal osteochondromatous proliferations<br />

4054 Myalgia eosinophilia <strong>as</strong>sociated with tryptophan

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