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Chondrodystrophic Myotonia (Schwartz-Jampel)
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Eaton Lambert (Myasthenic) Syndrome
Emery-Dreifuss Muscular Dystrophy (EDMD)
FacioScapuloHumeral MD (Landouzy-Dejerine) (FSH)
Fibre-Type Disproportion
Friedreich's Ataxia (FA)
Glycogen Storage Disease: Type I - (Von Gierke's Disease)
Glycogen Storage Disease: Type II - Acid Maltase Deficiency (Pompe's Disease)
Glycogen Storage Disease: Type III - Debrancher Enzyme Deficiency (Cori's or Forbe's Disease)
Glycogen Storage Disease: Type IV - Brancher Enzyme Deficiency (Andersen)
Glycogen Storage Disease: Type VI - Phosphfructokinase Deficiency (Tarui's Disease)
Glycogen Storage Disease: Type V - Phosphorylase Deficiency (McArdle's Disease)
Guillain Barre Syndrome
Hyperthyroid Myopathy (HYPTM & HYPOTM)
Hypertophic Type III - Dejerine-Sottas Disease
Idiopathic Myopathy
Inclusion Body Myositis (IBM)
Infective Myositis
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Lactate Dehydrogenase Deficiency
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Limb Girdle Muscular Dystrophy
Malignant Hyperthermia (Hyperpyrexia)
Mild Spinal Muscular Atrophy Type III - Juvenile Progressive Muscular Dystrophy (Kugelberg-Welander Disease)
Mini / Multi Core Disease
Mitochondrial Myopathy (MITO)
Motor Neurone Disease (ALS)
Muscular Dystrophy of Late Onset
Myasthenia Gravis (MG) Juvenile & Adult
Myoadenylate Deaminase Deficiency
Myotonia Congenita (MC) (Thomsen & Becker Disease)
Myotonic Dystrophy (MMD) (Steinert's Disease)
Myotubular (Centronuclear) Myopathy (MTM or CNM)
Nemaline Myopathy (NM)
Neuromyotonia (Isaacs)
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Periodic Paralysis (PP): Hyperkalaemic
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Periodic Paralysis OLD - Please Select Type!
Phosphofructokinase Deficiency (Tarui Disease)
Phosphoglycerate Kinase Deficiency
Phosphoglycerate Mutase Deficiency
Phosphorylase Deficiency (McArdle Disease)
Polymyositis (PM)
Pompe Disease
Pseudomyotonia
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Spinal Muscular Atrophy Type I [Severe] - Infantile Progressive (Werdnig-Hoffmann Disease)
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None
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Acid Maltase Deficiency (MPD or PYGM)
Amyotrophic Lateral Sclerosis (ALS)
Becker Muscular Dystrophy (BMD)
Benign Congenital Hypotonia (formally called Amyotonia Congenita)
Carnitine Deficiency (CD)
Carnitine Palmityl Transferase Deficiency (CPT)
Central Core Disease (CCD)
Charcot-Marie-Tooth Disease (CMT) or (Peroneal Muscular Atrophy)
Chondrodystrophic Myotonia (Schwartz-Jampel)
CIDP (Chronic Inflammatory Demyelinating Peripheral Neuropathy)
Congenital Muscular Dystrophy (Fukuyama)
Congenital Muscular Dystrophy (LMNA)
Congenital Muscular Dystrophy (Unspecified)
Congenital Myasthenic Syndrome (CMS)
Debrancher Enzyme Deficiency (DBD)
Dejerine-Sottas Disease (DS)
Dermatomyositis (DM)
Distal MD (DD)
Duchenne Muscular Dystrophy (Pseudohypertrophic)
Eaton Lambert (Myasthenic) Syndrome
Emery-Dreifuss Muscular Dystrophy (EDMD)
FacioScapuloHumeral MD (Landouzy-Dejerine) (FSH)
Fibre-Type Disproportion
Friedreich's Ataxia (FA)
Glycogen Storage Disease: Type I - (Von Gierke's Disease)
Glycogen Storage Disease: Type II - Acid Maltase Deficiency (Pompe's Disease)
Glycogen Storage Disease: Type III - Debrancher Enzyme Deficiency (Cori's or Forbe's Disease)
Glycogen Storage Disease: Type IV - Brancher Enzyme Deficiency (Andersen)
Glycogen Storage Disease: Type VI - Phosphfructokinase Deficiency (Tarui's Disease)
Glycogen Storage Disease: Type V - Phosphorylase Deficiency (McArdle's Disease)
Guillain Barre Syndrome
Hyperthyroid Myopathy (HYPTM & HYPOTM)
Hypertophic Type III - Dejerine-Sottas Disease
Idiopathic Myopathy
Inclusion Body Myositis (IBM)
Infective Myositis
Juvenile Dermatomyositis
Lactate Dehydrogenase Deficiency
Lambert-Eaton Syndrome (LES)
Limb Girdle Muscular Dystrophy
Malignant Hyperthermia (Hyperpyrexia)
Mild Spinal Muscular Atrophy Type III - Juvenile Progressive Muscular Dystrophy (Kugelberg-Welander Disease)
Mini / Multi Core Disease
Mitochondrial Myopathy (MITO)
Motor Neurone Disease (ALS)
Muscular Dystrophy of Late Onset
Myasthenia Gravis (MG) Juvenile & Adult
Myoadenylate Deaminase Deficiency
Myotonia Congenita (MC) (Thomsen & Becker Disease)
Myotonic Dystrophy (MMD) (Steinert's Disease)
Myotubular (Centronuclear) Myopathy (MTM or CNM)
Nemaline Myopathy (NM)
Neuromyotonia (Isaacs)
Ocular MD
Oculopharyngeal MD (OPMD)
Opthalmoplegic MD (Kearns-Sayre Syndrome)
Paramytonia Congenita (PC)
Periodic Paralysis (PP): Hyperkalaemic
Periodic Paralysis (PP): Hypokalaemic
Periodic Paralysis (PP): Normokalaemic
Periodic Paralysis OLD - Please Select Type!
Phosphofructokinase Deficiency (Tarui Disease)
Phosphoglycerate Kinase Deficiency
Phosphoglycerate Mutase Deficiency
Phosphorylase Deficiency (McArdle Disease)
Polymyositis (PM)
Pompe Disease
Pseudomyotonia
Spinal Bulbar Muscular Atrophy (SBMA) (Kennedy's Disease & X-Linked SBMA)
Spinal Muscular Atrophy (Aran-Duchenne Type) Adult Progressive
Spinal Muscular Atrophy Adult
Spinal Muscular Atrophy Juvenile (SMA Type 3)
Spinal Muscular Atrophy Type I [Severe] - Infantile Progressive (Werdnig-Hoffmann Disease)
Spinal Muscular Atrophy Type 2
Spino Cerebellar Ataxia
Type IV - X-linked Charcot-Marie-Tooth Disease
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1922
1921
1920
MD Type
*
Select
None
Unknown MD Type
Acid Maltase Deficiency (MPD or PYGM)
Amyotrophic Lateral Sclerosis (ALS)
Becker Muscular Dystrophy (BMD)
Benign Congenital Hypotonia (formally called Amyotonia Congenita)
Carnitine Deficiency (CD)
Carnitine Palmityl Transferase Deficiency (CPT)
Central Core Disease (CCD)
Charcot-Marie-Tooth Disease (CMT) or (Peroneal Muscular Atrophy)
Chondrodystrophic Myotonia (Schwartz-Jampel)
CIDP (Chronic Inflammatory Demyelinating Peripheral Neuropathy)
Congenital Muscular Dystrophy (Fukuyama)
Congenital Muscular Dystrophy (LMNA)
Congenital Muscular Dystrophy (Unspecified)
Congenital Myasthenic Syndrome (CMS)
Debrancher Enzyme Deficiency (DBD)
Dejerine-Sottas Disease (DS)
Dermatomyositis (DM)
Distal MD (DD)
Duchenne Muscular Dystrophy (Pseudohypertrophic)
Eaton Lambert (Myasthenic) Syndrome
Emery-Dreifuss Muscular Dystrophy (EDMD)
FacioScapuloHumeral MD (Landouzy-Dejerine) (FSH)
Fibre-Type Disproportion
Friedreich's Ataxia (FA)
Glycogen Storage Disease: Type I - (Von Gierke's Disease)
Glycogen Storage Disease: Type II - Acid Maltase Deficiency (Pompe's Disease)
Glycogen Storage Disease: Type III - Debrancher Enzyme Deficiency (Cori's or Forbe's Disease)
Glycogen Storage Disease: Type IV - Brancher Enzyme Deficiency (Andersen)
Glycogen Storage Disease: Type VI - Phosphfructokinase Deficiency (Tarui's Disease)
Glycogen Storage Disease: Type V - Phosphorylase Deficiency (McArdle's Disease)
Guillain Barre Syndrome
Hyperthyroid Myopathy (HYPTM & HYPOTM)
Hypertophic Type III - Dejerine-Sottas Disease
Idiopathic Myopathy
Inclusion Body Myositis (IBM)
Infective Myositis
Juvenile Dermatomyositis
Lactate Dehydrogenase Deficiency
Lambert-Eaton Syndrome (LES)
Limb Girdle Muscular Dystrophy
Malignant Hyperthermia (Hyperpyrexia)
Mild Spinal Muscular Atrophy Type III - Juvenile Progressive Muscular Dystrophy (Kugelberg-Welander Disease)
Mini / Multi Core Disease
Mitochondrial Myopathy (MITO)
Motor Neurone Disease (ALS)
Muscular Dystrophy of Late Onset
Myasthenia Gravis (MG) Juvenile & Adult
Myoadenylate Deaminase Deficiency
Myotonia Congenita (MC) (Thomsen & Becker Disease)
Myotonic Dystrophy (MMD) (Steinert's Disease)
Myotubular (Centronuclear) Myopathy (MTM or CNM)
Nemaline Myopathy (NM)
Neuromyotonia (Isaacs)
Ocular MD
Oculopharyngeal MD (OPMD)
Opthalmoplegic MD (Kearns-Sayre Syndrome)
Paramytonia Congenita (PC)
Periodic Paralysis (PP): Hyperkalaemic
Periodic Paralysis (PP): Hypokalaemic
Periodic Paralysis (PP): Normokalaemic
Periodic Paralysis OLD - Please Select Type!
Phosphofructokinase Deficiency (Tarui Disease)
Phosphoglycerate Kinase Deficiency
Phosphoglycerate Mutase Deficiency
Phosphorylase Deficiency (McArdle Disease)
Polymyositis (PM)
Pompe Disease
Pseudomyotonia
Spinal Bulbar Muscular Atrophy (SBMA) (Kennedy's Disease & X-Linked SBMA)
Spinal Muscular Atrophy (Aran-Duchenne Type) Adult Progressive
Spinal Muscular Atrophy Adult
Spinal Muscular Atrophy Juvenile (SMA Type 3)
Spinal Muscular Atrophy Type I [Severe] - Infantile Progressive (Werdnig-Hoffmann Disease)
Spinal Muscular Atrophy Type 2
Spino Cerebellar Ataxia
Type IV - X-linked Charcot-Marie-Tooth Disease
Other
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1920
MD Type
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Unknown MD Type
Acid Maltase Deficiency (MPD or PYGM)
Amyotrophic Lateral Sclerosis (ALS)
Becker Muscular Dystrophy (BMD)
Benign Congenital Hypotonia (formally called Amyotonia Congenita)
Carnitine Deficiency (CD)
Carnitine Palmityl Transferase Deficiency (CPT)
Central Core Disease (CCD)
Charcot-Marie-Tooth Disease (CMT) or (Peroneal Muscular Atrophy)
Chondrodystrophic Myotonia (Schwartz-Jampel)
CIDP (Chronic Inflammatory Demyelinating Peripheral Neuropathy)
Congenital Muscular Dystrophy (Fukuyama)
Congenital Muscular Dystrophy (LMNA)
Congenital Muscular Dystrophy (Unspecified)
Congenital Myasthenic Syndrome (CMS)
Debrancher Enzyme Deficiency (DBD)
Dejerine-Sottas Disease (DS)
Dermatomyositis (DM)
Distal MD (DD)
Duchenne Muscular Dystrophy (Pseudohypertrophic)
Eaton Lambert (Myasthenic) Syndrome
Emery-Dreifuss Muscular Dystrophy (EDMD)
FacioScapuloHumeral MD (Landouzy-Dejerine) (FSH)
Fibre-Type Disproportion
Friedreich's Ataxia (FA)
Glycogen Storage Disease: Type I - (Von Gierke's Disease)
Glycogen Storage Disease: Type II - Acid Maltase Deficiency (Pompe's Disease)
Glycogen Storage Disease: Type III - Debrancher Enzyme Deficiency (Cori's or Forbe's Disease)
Glycogen Storage Disease: Type IV - Brancher Enzyme Deficiency (Andersen)
Glycogen Storage Disease: Type VI - Phosphfructokinase Deficiency (Tarui's Disease)
Glycogen Storage Disease: Type V - Phosphorylase Deficiency (McArdle's Disease)
Guillain Barre Syndrome
Hyperthyroid Myopathy (HYPTM & HYPOTM)
Hypertophic Type III - Dejerine-Sottas Disease
Idiopathic Myopathy
Inclusion Body Myositis (IBM)
Infective Myositis
Juvenile Dermatomyositis
Lactate Dehydrogenase Deficiency
Lambert-Eaton Syndrome (LES)
Limb Girdle Muscular Dystrophy
Malignant Hyperthermia (Hyperpyrexia)
Mild Spinal Muscular Atrophy Type III - Juvenile Progressive Muscular Dystrophy (Kugelberg-Welander Disease)
Mini / Multi Core Disease
Mitochondrial Myopathy (MITO)
Motor Neurone Disease (ALS)
Muscular Dystrophy of Late Onset
Myasthenia Gravis (MG) Juvenile & Adult
Myoadenylate Deaminase Deficiency
Myotonia Congenita (MC) (Thomsen & Becker Disease)
Myotonic Dystrophy (MMD) (Steinert's Disease)
Myotubular (Centronuclear) Myopathy (MTM or CNM)
Nemaline Myopathy (NM)
Neuromyotonia (Isaacs)
Ocular MD
Oculopharyngeal MD (OPMD)
Opthalmoplegic MD (Kearns-Sayre Syndrome)
Paramytonia Congenita (PC)
Periodic Paralysis (PP): Hyperkalaemic
Periodic Paralysis (PP): Hypokalaemic
Periodic Paralysis (PP): Normokalaemic
Periodic Paralysis OLD - Please Select Type!
Phosphofructokinase Deficiency (Tarui Disease)
Phosphoglycerate Kinase Deficiency
Phosphoglycerate Mutase Deficiency
Phosphorylase Deficiency (McArdle Disease)
Polymyositis (PM)
Pompe Disease
Pseudomyotonia
Spinal Bulbar Muscular Atrophy (SBMA) (Kennedy's Disease & X-Linked SBMA)
Spinal Muscular Atrophy (Aran-Duchenne Type) Adult Progressive
Spinal Muscular Atrophy Adult
Spinal Muscular Atrophy Juvenile (SMA Type 3)
Spinal Muscular Atrophy Type I [Severe] - Infantile Progressive (Werdnig-Hoffmann Disease)
Spinal Muscular Atrophy Type 2
Spino Cerebellar Ataxia
Type IV - X-linked Charcot-Marie-Tooth Disease
Other
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Acid Maltase Deficiency (MPD or PYGM)
Amyotrophic Lateral Sclerosis (ALS)
Becker Muscular Dystrophy (BMD)
Benign Congenital Hypotonia (formally called Amyotonia Congenita)
Carnitine Deficiency (CD)
Carnitine Palmityl Transferase Deficiency (CPT)
Central Core Disease (CCD)
Charcot-Marie-Tooth Disease (CMT) or (Peroneal Muscular Atrophy)
Chondrodystrophic Myotonia (Schwartz-Jampel)
CIDP (Chronic Inflammatory Demyelinating Peripheral Neuropathy)
Congenital Muscular Dystrophy (Fukuyama)
Congenital Muscular Dystrophy (LMNA)
Congenital Muscular Dystrophy (Unspecified)
Congenital Myasthenic Syndrome (CMS)
Debrancher Enzyme Deficiency (DBD)
Dejerine-Sottas Disease (DS)
Dermatomyositis (DM)
Distal MD (DD)
Duchenne Muscular Dystrophy (Pseudohypertrophic)
Eaton Lambert (Myasthenic) Syndrome
Emery-Dreifuss Muscular Dystrophy (EDMD)
FacioScapuloHumeral MD (Landouzy-Dejerine) (FSH)
Fibre-Type Disproportion
Friedreich's Ataxia (FA)
Glycogen Storage Disease: Type I - (Von Gierke's Disease)
Glycogen Storage Disease: Type II - Acid Maltase Deficiency (Pompe's Disease)
Glycogen Storage Disease: Type III - Debrancher Enzyme Deficiency (Cori's or Forbe's Disease)
Glycogen Storage Disease: Type IV - Brancher Enzyme Deficiency (Andersen)
Glycogen Storage Disease: Type VI - Phosphfructokinase Deficiency (Tarui's Disease)
Glycogen Storage Disease: Type V - Phosphorylase Deficiency (McArdle's Disease)
Guillain Barre Syndrome
Hyperthyroid Myopathy (HYPTM & HYPOTM)
Hypertophic Type III - Dejerine-Sottas Disease
Idiopathic Myopathy
Inclusion Body Myositis (IBM)
Infective Myositis
Juvenile Dermatomyositis
Lactate Dehydrogenase Deficiency
Lambert-Eaton Syndrome (LES)
Limb Girdle Muscular Dystrophy
Malignant Hyperthermia (Hyperpyrexia)
Mild Spinal Muscular Atrophy Type III - Juvenile Progressive Muscular Dystrophy (Kugelberg-Welander Disease)
Mini / Multi Core Disease
Mitochondrial Myopathy (MITO)
Motor Neurone Disease (ALS)
Muscular Dystrophy of Late Onset
Myasthenia Gravis (MG) Juvenile & Adult
Myoadenylate Deaminase Deficiency
Myotonia Congenita (MC) (Thomsen & Becker Disease)
Myotonic Dystrophy (MMD) (Steinert's Disease)
Myotubular (Centronuclear) Myopathy (MTM or CNM)
Nemaline Myopathy (NM)
Neuromyotonia (Isaacs)
Ocular MD
Oculopharyngeal MD (OPMD)
Opthalmoplegic MD (Kearns-Sayre Syndrome)
Paramytonia Congenita (PC)
Periodic Paralysis (PP): Hyperkalaemic
Periodic Paralysis (PP): Hypokalaemic
Periodic Paralysis (PP): Normokalaemic
Periodic Paralysis OLD - Please Select Type!
Phosphofructokinase Deficiency (Tarui Disease)
Phosphoglycerate Kinase Deficiency
Phosphoglycerate Mutase Deficiency
Phosphorylase Deficiency (McArdle Disease)
Polymyositis (PM)
Pompe Disease
Pseudomyotonia
Spinal Bulbar Muscular Atrophy (SBMA) (Kennedy's Disease & X-Linked SBMA)
Spinal Muscular Atrophy (Aran-Duchenne Type) Adult Progressive
Spinal Muscular Atrophy Adult
Spinal Muscular Atrophy Juvenile (SMA Type 3)
Spinal Muscular Atrophy Type I [Severe] - Infantile Progressive (Werdnig-Hoffmann Disease)
Spinal Muscular Atrophy Type 2
Spino Cerebellar Ataxia
Type IV - X-linked Charcot-Marie-Tooth Disease
Other
Relationship to Member
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