|
Mitochondrial Complex 1 Deficiency |
Chain1040 |
This is a rare disease. |
|
Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form |
Chain1041 |
This is a rare disease. |
|
Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form Cystathioninuria |
Chain1042 |
This is a rare disease. |
|
Mitochondrial HMG-CoA Synthase Deficiency |
Chain1043 |
This is a rare disease. |
|
Mitochondrial Myopathy and Sideroblastic Anemia |
Chain1044 |
This is a rare disease. |
|
Mitochondrial Neurogastrointestinal Encephalopathy Syndrome without Leukoencephalopathy |
Chain1045 |
This is a rare disease. |
|
Mitochondrial Neurogastrointestinal Encephalopathy Syndrome without Leukoencephalopathy, Autosomal Recessive |
Chain1046 |
This is a rare disease. |
|
Mitomycin-C resistance |
Chain1047 |
This is a rare disease. |
|
Miyoshi Myopathy (Analysis A) |
Chain1048 |
This is a rare disease. |
|
Miyoshi Myopathy (Analysis B) |
Chain1049 |
This is a rare disease. |
|
Miyoshi Myopathy (Analysis C) |
Chain1050 |
This is a rare disease. |
|
Limb Girdle Muscular Dystrophy, Type 2B (Analysis A) |
Chain1051 |
This is a rare disease. |
|
Limb Girdle Muscular Dystrophy, Type 2B (Analysis B) |
Chain1052 |
This is a rare disease. |
|
Distal Myopathy with Anterior Tibial Onset |
Chain1053 |
This is a rare disease. |
|
MNGIE Syndrome |
Chain1054 |
This is a rare disease. |
|
Modifier of Erythropoietic Protoporphyria |
Chain1055 |
This is a rare disease. |
|
Modifier of Hemochromatosis, Type 1 |
Chain1056 |
This is a rare disease. |
|
Modifier of Iron Overload |
Chain1057 |
This is a rare disease. |
|
Modifier of Marfan Syndrome, Type II |
Chain1058 |
This is a rare disease. |
|
Modifier of Parkinson's Disease Age of Onset |
Chain1059 |
This is a rare disease. |
|
Muscular dystrophy, Duchenne |
Chain1094 |
This is a rare disease. |
|
Modulator of MARK1 Transcription |
Chain1061 |
This is a rare disease. |
|
Muscular dystrophy, limb girdle |
Chain1096 |
This is a rare disease. |
|
Fast progression of HIV disease |
Chain1063 |
This is a rare disease. |
|
More severe liver inflammation and fibrosis with HCV Infection |
Chain1064 |
This is a rare disease. |
|
Mental Retardation, X-linked 93 |
Chain1066 |
This is a rare disease. |
|
Mucolipidosis II, Alpha/Beta |
Chain1067 |
This is a rare disease. |
|
Mucolipidosis III, Alpha/Beta |
Chain1068 |
This is a rare disease. |
|
Mucolipidosis III, Gamma |
Chain1069 |
This is a rare disease. |
|
Mucolipidosis IV |
Chain1070 |
This is a rare disease. |
|
Mucopolysaccharidosis Type II |
Chain1071 |
This is a rare disease. |
|
Multi-minicore Disease |
Chain1073 |
This is a rare disease. |
|
Multiple cancers |
Chain1074 |
This is a rare disease. |
|
Multiple Carboxylase Deficiency, Biotin-responsive |
Chain1075 |
This is a rare disease. |
|
Multiple Cutaneous and Uterine Leiomyomata (Analysis A) |
Chain1076 |
This is a rare disease. |