| Diseases |
Alias |
|
| Mitochondrial Myopathy |
|
|
| Mitochondrial Disease |
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Mitochondrial Diseases
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Mitochondrial Disorder
|
|
| Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes |
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Melas Syndrome
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MELAS
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Mitochondrial Encephalomyopathy Lactic Acidosis And Stroke-Like Episodes
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Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode
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Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes
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Myopathy, Mitochondrial-Encephalopathy-Lactic Acidosis-Stroke
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Mitochondrial Encephalomyopathy, Lactic Acidosis And Stroke-Like Episodes
-
Mitochondrial Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes
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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis And Stroke-Like Episodes
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Mitochondrial Encephalomyopathy With Lactic Acidosis And Stroke-Like Episodes Syndrome
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Myopathy, Mitochondrial, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes
|
|
| Lipomatosis, Multiple Symmetric |
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Multiple Symmetric Lipomatosis
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Lipomatosis, Familial Benign Cervical
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Lipomatosis, Multiple Symmetrical
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Lipodystrophy, Cephalothoracic
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Benign Symmetrical Lipomatosis
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Madelung Disease
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Madelung'S Disease
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MSL
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Cervical Symmetrical Lipomatosis
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Launois-Bensaude'S Lipomatosis
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Madelung'S Neck
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Multiple Symmetrical Lipomatosis
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Familial Symmetric Lipomatosis
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Launois-Bensaude Syndrome
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Cephalothoracic Lipodystrophy
-
Familial Benign Cervical Lipomatosis
-
Launois-Bensaude Lipomatosis
|
|
| Motor Neuron Disease |
-
Anterior Horn Cell Disease
-
Motor Neuron Diseases
-
Mnd - [Motor Neurone Disease]
-
Lou Gehrig Disease
-
Creeping Palsy
-
Creeping Paralysis
-
Bulbar Motor Neuron Disease
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Bulbar Syndrome
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Anterior Horn Cell Disorder
-
Hereditary Motor Neuron Disease
|
|
| Leber Hereditary Optic Neuropathy, Modifier Of |
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Leber Optic Atrophy
-
Leber Hereditary Optic Neuropathy
-
LHON
-
Leber'S Hereditary Optic Neuropathy
-
Leber Optic Atrophy, Susceptibility To
-
Leber'S Optic Atrophy
-
LOAM
-
Loas
-
Leber'S Disease
-
Leber'S Optic Neuropathy
-
Optic Atrophy, Hereditary, Leber
-
Lhon, Modifier Of
-
Optic Atrophy, Leber Type
-
Hereditary Optic Neuroretinopathy
-
Leber Hereditary Optic Atrophy
-
Loa
-
Optic Atrophy Leber Type
-
Leber Hereditary Optic Neuropathy, Modifier
-
Leber Hereditary Optic Neuropathy Susceptibility
-
Modifier Of Leber Hereditary Optic Neuropathy
-
Lebers Hereditary Optic Neuropathy
-
Leber Congenital Amaurosis
|
|
| Leber Plus Disease |
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Leber Congenital Amaurosis
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Lca
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Leber'S Amaurosis
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Leber'S Disease
-
Amaurosis Congenita Of Leber
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Amaurosis Congenita Of Leber, Type 1
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Lhon Plus Disease
-
Congenital Absence Of The Rods And Cones
-
Congenital Retinal Blindness
-
Crb
-
Congenital Amaurosis Of Retinal Origin
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Leber'S Congenital Amaurosis
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Leber Congenital Amaurosis 1
-
Leber'S Congenital Tapetoretinal Degeneration
-
Leber'S Congenital Tapetoretinal Dysplasia
-
Lca1
-
Leber Congenital Amaurosis Type 1
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Retinal Blindness, Congenital
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Amaurosis, Leber Congenital
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Dysgenesis Neuroepithelialis Retinae
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Hereditary Epithelial Dysplasia Of Retina
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Hereditary Retinal Aplasia
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Heredoretinopathia Congenitalis
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Leber Abiotrophy
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Leber Congenital Tapetoretinal Degeneration
-
Lebers Congenital Amaurosis
-
Optic Atrophy, Hereditary, Leber
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