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| Boli A-Z | | Acquired Generalized Lipodystrophy
Adducted Thumbs Dundar Type
Adie Pupil
Adrenomyodystrophy
Adult Dermatomyositis
Adult-Onset Nemaline Myopathy
Adult Progressive Spinal Muscular Atrophy Aran Duchenne Type
Amyotrophy, Monomelic
Anterior Cruciate Ligament Tears
Arthrogryposis, Distal, Type 10
Arthrogryposis, Distal, Type 1a
Arthrogryposis, Distal, Type 1b
Arthrogryposis, Distal, Type 2a
Arthrogryposis, Distal, Type 2e
Arthrogryposis, Distal, Type 3
Arthrogryposis, Distal, Type 4
Arthrogryposis, Distal, Type 5
Arthrogryposis, Distal, Type 5d
Arthrogryposis, Distal, Type 6
Arthrogryposis, Distal, Type 7
Arthrogryposis, Distal, Type 8
Arthrogryposis, Distal, Type 9
Arthrogryposis Spinal Muscular Atrophy
Atrophic Muscular Disease
Autoimmune Disease of Musculoskeletal System
Autoinflammation, Lipodystrophy, and Dermatosis Syndrome
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to Dgat2 Mutation
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to Kif5a Mutation
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due to Tfg Mutation
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2g
Autosomal Dominant Childhood-Onset Proximal Spinal Muscular Atrophy
Autosomal Dominant Intermediate Charcot-Marie-Tooth
Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type B
Autosomal Dominant Limb-Girdle Muscular Dystrophy
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1c
Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1g
Autosomal Dominant Progressive External Ophthalmoplegia
Autosomal Recessive Intermediate Charcot-Marie-Tooth Disease
Autosomal Recessive Limb-Girdle Muscular Dystrophy
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2b
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2e
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2h
Bacterial Myositis
Bassoe Syndrome
Benign Autosomal Dominant Myopathy
Bethlem Myopathy 1
Bethlem Myopathy 2
Bicipital Tenosynovitis
Brain Malformation-Musculoskeletal Abnormalities-Facial Dysmorphism-Intellectual Disability Syndrome
Broad Ligament Malignant Neoplasm
Brown's Tendon Sheath Syndrome
Brown Syndrome
Calcific Tendinitis
Camptodactyly with Muscular Hypoplasia, Skeletal Dysplasia, and Abnormal Palmar Creases
Celiac Artery Stenosis from Compression by Median Arcuate Ligament of Diaphragm
Central Core Disease of Muscle
Central Core Myopathy
Centronuclear Myopathy
Cerebellar Ataxia, Early-Onset, with Retained Tendon Reflexes
Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease, Demyelinating, Type 1a
Charcot-Marie-Tooth Disease, Demyelinating, Type 1b
Charcot-Marie-Tooth Disease, Demyelinating, Type 1c
Charcot-Marie-Tooth Disease, Demyelinating, Type 1d
Charcot-Marie-Tooth Disease, Demyelinating, Type 1f
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
Charcot-Marie-Tooth Disease, Dominant Intermediate a
Charcot-Marie-Tooth Disease, Dominant Intermediate B
Charcot-Marie-Tooth Disease, Dominant Intermediate C
Charcot-Marie-Tooth Disease Intermediate Type
Charcot-Marie-Tooth Disease, Recessive Intermediate a
Charcot-Marie-Tooth Disease, Recessive Intermediate B
Charcot-Marie-Tooth Disease, Recessive Intermediate C
Charcot-Marie-Tooth Disease Type 2a
Charcot-Marie-Tooth Disease Type 2a2
Charcot-Marie-Tooth Disease Type 2c
Charcot-Marie-Tooth Disease Type 2f
Charcot-Marie-Tooth Disease Type 2g
Charcot-Marie-Tooth Disease Type 2k
Charcot-Marie-Tooth Disease Type 2l
Charcot-Marie-Tooth Disease Type 2n
Charcot-Marie-Tooth Disease Type 2o
Charcot-Marie-Tooth Disease Type 2q
Charcot-Marie-Tooth Disease, Type 4a
Charcot-Marie-Tooth Disease, Type 4b1
Charcot-Marie-Tooth Disease, Type 4b2
Charcot-Marie-Tooth Disease, Type 4b3
Charcot-Marie-Tooth Disease, Type 4c
Charcot-Marie-Tooth Disease, Type 4d
Charcot-Marie-Tooth Disease, Type 4h
Charcot-Marie-Tooth Disease, Type 4j
Charcot-Marie-Tooth Disease, Type 4k
Charcot-Marie-Tooth Disease Type 5
Charcot-Marie-Tooth Disease Type 7
Charcot-Marie-Tooth Disease, X-Linked Dominant, 1
Charcot-Marie-Tooth Disease, X-Linked Dominant, 6
Charcot-Marie-Tooth Disease, X-Linked Recessive, 2
Charcot-Marie-Tooth Disease, X-Linked Recessive, 3
Charcot-Marie-Tooth Disease, X-Linked Recessive, 5
Charcot-Marie-Tooth Peroneal Muscular Atrophy and Friedreich Ataxia, Combined
Charcot-Marie-Tooth Peroneal Muscular Atrophy, X-Linked, with Aplasia Cutis Congenita
Childhood Type Dermatomyositis
Chronic Progressive External Ophthalmoplegia
Collagen Vi Related Muscular Dystrophy
Congenital Benign Spinal Muscular Atrophy Dominant
Congenital Disorder of Glycosylation, Type Ia
Congenital Disorder of Glycosylation, Type Ib
Congenital Disorder of Glycosylation, Type Ic
Congenital Disorder of Glycosylation, Type Id
Congenital Disorder of Glycosylation, Type Ie
Congenital Disorder of Glycosylation, Type if
Congenital Disorder of Glycosylation, Type Ig
Congenital Disorder of Glycosylation, Type Ih
Congenital Disorder of Glycosylation, Type Ii
Congenital Disorder of Glycosylation, Type Iia
Congenital Disorder of Glycosylation, Type Iib
Congenital Disorder of Glycosylation, Type Iic
Congenital Disorder of Glycosylation, Type Iid
Congenital Disorder of Glycosylation, Type Iif
Congenital Disorder of Glycosylation, Type Iig
Congenital Disorder of Glycosylation, Type Iih
Congenital Disorder of Glycosylation, Type Iii
Congenital Disorder of Glycosylation, Type I/iix
Congenital Disorder of Glycosylation, Type Iij
Congenital Disorder of Glycosylation, Type Iik
Congenital Disorder of Glycosylation, Type Iil
Congenital Disorder of Glycosylation, Type Iim
Congenital Disorder of Glycosylation, Type Iin
Congenital Disorder of Glycosylation, Type Iio
Congenital Disorder of Glycosylation, Type Iip
Congenital Disorder of Glycosylation, Type Iiq
Congenital Disorder of Glycosylation, Type Ij
Congenital Disorder of Glycosylation, Type Ik
Congenital Disorder of Glycosylation, Type Il
Congenital Disorder of Glycosylation, Type Im
Congenital Disorder of Glycosylation, Type in
Congenital Disorder of Glycosylation, Type Io
Congenital Disorder of Glycosylation, Type Ip
Congenital Disorder of Glycosylation, Type Iq
Congenital Disorder of Glycosylation, Type Ir
Congenital Disorder of Glycosylation, Type It
Congenital Disorder of Glycosylation, Type Iu
Congenital Disorder of Glycosylation, Type Iw
Congenital Disorder of Glycosylation, Type Ix
Congenital Disorder of Glycosylation, Type Iy
Congenital Fiber-Type Disproportion
Congenital Generalized Lipodystrophy
Congenital Muscular Alpha-Dystroglycanopathy with Brain and Eye Anomalies
Congenital Muscular Dystrophy Due to Dystroglycanopathy
Congenital Muscular Dystrophy-Dystroglycanopathy with or Without Intellectual Disability
Congenital Muscular Dystrophy Type 1a
Congenital Muscular Dystrophy with Cerebellar Involvement
Congenital Muscular Dystrophy with Hyperlaxity
Congenital Muscular Dystrophy with Intellectual Disability
Congenital Muscular Dystrophy Without Intellectual Disability
Congenital Structural Myopathy
Congenital Torticollis
Cornelia De Lange Syndrome
Cornelia De Lange Syndrome 1
Cornelia De Lange Syndrome 2
Cornelia De Lange Syndrome 3
Cornelia De Lange Syndrome 4
Cornelia De Lange Syndrome 5
Costocoracoid Ligament, Congenitally Short
Cylindrical Spirals Myopathy
Cyprus Facial Neuromusculoskeletal Syndrome
De Quervain Disease
Dermatomyositis
Desmoid Tumor
Diaphragmatic Eventration
Diaphragmatic Hernia 2
Diaphragmatic Hernia 3
Diaphragmatic Hernia, Congenital
Diaphragm Disease
Distal Arthrogryposis
Distal Hereditary Motor Neuropathies
Distal Hereditary Motor Neuropathy Type 7
Distal Hereditary Motor Neuropathy, Type Ii
Distal Hereditary Motor Neuropathy, Type V
Distal Muscular Dystrophy
Dystonia
Dystonia 12
Dystonia 13, Torsion, Autosomal Dominant
Dystonia 16
Dystonia 17, Torsion, Autosomal Recessive
Dystonia 1, Torsion, Autosomal Dominant
Dystonia 21
Dystonia 23
Dystonia 24
Dystonia 25
Dystonia 27
Dystonia 2, Torsion, Autosomal Recessive
Dystonia 3, Torsion, X-Linked
Dystonia 4, Torsion, Autosomal Dominant
Dystonia 6, Torsion
Dystonia 7, Torsion
Dystonia 9
Dystonia, Juvenile-Onset
Early-Onset Generalized Dystonia
Early-Onset Generalized Limb-Onset Dystonia
Early-Onset Progressive Encephalopathy-Spastic Ataxia-Distal Spinal Muscular Atrophy Syndrome
Ehlers-Danlos Syndrome, Musculocontractural Type, 1
Ehlers-Danlos Syndrome, Musculocontractural Type, 2
Emery-Dreifuss Muscular Dystrophy
Emery-Dreifuss Muscular Dystrophy 1, X-Linked
Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant
Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive
Emery-Dreifuss Muscular Dystrophy 4, Autosomal Dominant
Emery-Dreifuss Muscular Dystrophy 5, Autosomal Dominant
Emery-Dreifuss Muscular Dystrophy 7, Autosomal Dominant
Emery-Dreifuss Muscular Dystrophy, Dominant Type
Emery-Dreifuss Muscular Dystrophy, X-Linked
Emery-Dreifuss Syndrome
Endomyocardial Fibrosis
Epidermolysa Bullosa Simplex with Muscular Dystrophy
Epidermolysis Bullosa Simplex with Muscular Dystrophy
Epileptic Encephalopathy, Early Infantile, 1
Epileptic Encephalopathy, Early Infantile, 11
Epileptic Encephalopathy, Early Infantile, 12
Epileptic Encephalopathy, Early Infantile, 13
Epileptic Encephalopathy, Early Infantile, 14
Epileptic Encephalopathy, Early Infantile, 15
Epileptic Encephalopathy, Early Infantile, 16
Epileptic Encephalopathy, Early Infantile, 17
Epileptic Encephalopathy, Early Infantile, 18
Epileptic Encephalopathy, Early Infantile, 19
Epileptic Encephalopathy, Early Infantile, 2
Epileptic Encephalopathy, Early Infantile, 21
Epileptic Encephalopathy, Early Infantile, 23
Epileptic Encephalopathy, Early Infantile, 24
Epileptic Encephalopathy, Early Infantile, 25
Epileptic Encephalopathy, Early Infantile, 26
Epileptic Encephalopathy, Early Infantile, 27
Epileptic Encephalopathy, Early Infantile, 28
Epileptic Encephalopathy, Early Infantile, 29
Epileptic Encephalopathy, Early Infantile, 3
Epileptic Encephalopathy, Early Infantile, 30
Epileptic Encephalopathy, Early Infantile, 31
Epileptic Encephalopathy, Early Infantile, 32
Epileptic Encephalopathy, Early Infantile, 33
Epileptic Encephalopathy, Early Infantile, 34
Epileptic Encephalopathy, Early Infantile, 35
Epileptic Encephalopathy, Early Infantile, 36
Epileptic Encephalopathy, Early Infantile, 37
Epileptic Encephalopathy, Early Infantile, 38
Epileptic Encephalopathy, Early Infantile, 39
Epileptic Encephalopathy, Early Infantile, 4
Epileptic Encephalopathy, Early Infantile, 40
Epileptic Encephalopathy, Early Infantile, 41
Epileptic Encephalopathy, Early Infantile, 42
Epileptic Encephalopathy, Early Infantile, 43
Epileptic Encephalopathy, Early Infantile, 44
Epileptic Encephalopathy, Early Infantile, 45
Epileptic Encephalopathy, Early Infantile, 46
Epileptic Encephalopathy, Early Infantile, 47
Epileptic Encephalopathy, Early Infantile, 48
Epileptic Encephalopathy, Early Infantile, 49
Epileptic Encephalopathy, Early Infantile, 5
Epileptic Encephalopathy, Early Infantile, 50
Epileptic Encephalopathy, Early Infantile, 51
Epileptic Encephalopathy, Early Infantile, 52
Epileptic Encephalopathy, Early Infantile, 53
Epileptic Encephalopathy, Early Infantile, 54
Epileptic Encephalopathy, Early Infantile, 55
Epileptic Encephalopathy, Early Infantile, 56
Epileptic Encephalopathy, Early Infantile, 57
Epileptic Encephalopathy, Early Infantile, 58
Epileptic Encephalopathy, Early Infantile, 6
Epileptic Encephalopathy, Early Infantile, 7
Epileptic Encephalopathy, Early Infantile, 8
Epileptic Encephalopathy, Early Infantile, 9
Facioscapulohumeral Muscular Dystrophy 1
Facioscapulohumeral Muscular Dystrophy 2
Fibular Collateral Ligament Bursitis
Fukuyama Type Muscular Dystrophy
Ganglion or Cyst of Synovium/tendon/bursa
Glycogen Storage Disease
Glycogen Storage Disease Ia
Glycogen Storage Disease Ib
Glycogen Storage Disease Ic
Glycogen Storage Disease Ii
Glycogen Storage Disease Iii
Glycogen Storage Disease Iv
Glycogen Storage Disease Ix
Glycogen Storage Disease Ixa
Glycogen Storage Disease Ixb
Glycogen Storage Disease Ixc
Glycogen Storage Disease Type 0
Glycogen Storage Disease, Type Ixd
Glycogen Storage Disease V
Glycogen Storage Disease Vi
Glycogen Storage Disease Vii
Glycogen Storage Disease Viii
Glycogen Storage Disease X
Glycogen Storage Disease Xii
Glycogen Storage Disease Xiii
Glycogen Storage Disease Xv
Gne-Related Myopathy
Granulomatous Myositis
Harding Ataxia
Hereditary Dystonia
Hereditary Motor and Sensory Neuropathy, Type Iic
Hereditary Motor and Sensory Neuropathy V
Hernia, Anterior Diaphragmatic
Hypertrophia Musculorum Vera
Hypotonic Sclerotic Muscular Dystrophy
Inclusion Body Myositis
Infantile Epileptic Encephalopathy
Intermediate Congenital Nemaline Myopathy
Jankovic Rivera Syndrome
Juvenile Spinal Muscular Atrophy
Juvenile Temporal Arteritis
Kearns-Sayre Syndrome
Kocher-Debre-Semelaigne Syndrome
Lama2-Related Muscular Dystrophy
Limb-Girdle Muscular Dystrophy
Limb-Girdle Muscular Dystrophy, Type 1g
Lipodystrophy, Congenital Generalized, Type 1
Lipodystrophy, Congenital Generalized, Type 2
Lipodystrophy, Congenital Generalized, Type 3
Lipodystrophy, Congenital Generalized, Type 4
Lissencephaly
Lissencephaly 1
Lissencephaly 2
Lissencephaly 3
Lissencephaly 4
Lissencephaly 5
Lissencephaly 8
Malignant Giant Cell Tumor of the Tendon Sheath
Masters-Allen Syndrome
Median Arcuate Ligament Syndrome
Melanoma of Soft Tissue
Menkes Disease
Mitochondrial Encephalomyopathy
Mitochondrial Myopathy
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes
Mitochondrial Myopathy, Infantile, Transient
Mitochondrial Neurogastrointestinal Encephalopathy Disease
Miyoshi Muscular Dystrophy 1
Miyoshi Muscular Dystrophy 2
Miyoshi Muscular Dystrophy 3
Motor Peripheral Neuropathy
Muscle Disorders
Muscle Eye Brain Disease
Muscle Tissue Disease
Muscular Atrophy
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus
Muscular Atrophy, Malignant Neurogenic
Muscular Dystrophy
Muscular Dystrophy, Adult-Onset, with Leukoencephalopathy
Muscular Dystrophy, Barnes Type
Muscular Dystrophy, Becker Type
Muscular Dystrophy, Cardiac Type
Muscular Dystrophy, Congenital, 1b
Muscular Dystrophy, Congenital, Davignon-Chauveau Type
Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency
Muscular Dystrophy, Congenital, Lmna-Related
Muscular Dystrophy, Congenital, Megaconial Type
Muscular Dystrophy, Congenital Merosin-Deficient, 1a
Muscular Dystrophy, Congenital, Merosin-Positive
Muscular Dystrophy, Congenital, Producing Arthrogryposis
Muscular Dystrophy, Congenital, with Cataracts and Intellectual Disability
Muscular Dystrophy, Congenital, with Cerebellar Atrophy
Muscular Dystrophy, Congenital, with Infantile Cataract and Hypogonadism
Muscular Dystrophy, Congenital, with Rapid Progression
Muscular Dystrophy, Congenital, with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers
Muscular Dystrophy, Duchenne and Becker Type
Muscular Dystrophy, Duchenne Type
Muscular Dystrophy-Dystroglycanopathy
Muscular Dystrophy-Dystroglycanopathy , Type a, 1
Muscular Dystrophy-Dystroglycanopathy , Type a, 10
Muscular Dystrophy-Dystroglycanopathy , Type a, 11
Muscular Dystrophy-Dystroglycanopathy , Type a, 12
Muscular Dystrophy-Dystroglycanopathy , Type a, 13
Muscular Dystrophy-Dystroglycanopathy , Type a, 14
Muscular Dystrophy-Dystroglycanopathy , Type a, 2
Muscular Dystrophy-Dystroglycanopathy , Type a, 3
Muscular Dystrophy-Dystroglycanopathy , Type a, 4
Muscular Dystrophy-Dystroglycanopathy , Type a, 5
Muscular Dystrophy-Dystroglycanopathy , Type a, 6
Muscular Dystrophy-Dystroglycanopathy , Type a, 7
Muscular Dystrophy-Dystroglycanopathy , Type a, 8
Muscular Dystrophy-Dystroglycanopathy , Type a, 9
Muscular Dystrophy-Dystroglycanopathy , Type B, 1
Muscular Dystrophy-Dystroglycanopathy , Type B, 14
Muscular Dystrophy-Dystroglycanopathy , Type B, 2
Muscular Dystrophy-Dystroglycanopathy , Type B, 3
Muscular Dystrophy-Dystroglycanopathy , Type B, 4
Muscular Dystrophy-Dystroglycanopathy , Type B, 5
Muscular Dystrophy-Dystroglycanopathy , Type B, 6
Muscular Dystrophy-Dystroglycanopathy , Type C, 1
Muscular Dystrophy-Dystroglycanopathy , Type C, 12
Muscular Dystrophy-Dystroglycanopathy , Type C, 14
Muscular Dystrophy-Dystroglycanopathy , Type C, 2
Muscular Dystrophy-Dystroglycanopathy , Type C, 3
Muscular Dystrophy-Dystroglycanopathy , Type C, 4
Muscular Dystrophy-Dystroglycanopathy , Type C, 5
Muscular Dystrophy-Dystroglycanopathy , Type C, 7
Muscular Dystrophy-Dystroglycanopathy , Type C, 9
Muscular Dystrophy, Hemizygous Lethal Type
Muscular Dystrophy, Limb-Girdle, Type 1a
Muscular Dystrophy, Limb-Girdle, Type 1b
Muscular Dystrophy, Limb-Girdle, Type 1c
Muscular Dystrophy, Limb-Girdle, Type 1e
Muscular Dystrophy, Limb-Girdle, Type 1f
Muscular Dystrophy, Limb-Girdle, Type 1h
Muscular Dystrophy, Limb-Girdle, Type 2a
Muscular Dystrophy Limb Girdle Type 2a, Erb Type
Muscular Dystrophy, Limb-Girdle, Type 2b
Muscular Dystrophy, Limb-Girdle, Type 2c
Muscular Dystrophy, Limb-Girdle, Type 2d
Muscular Dystrophy, Limb-Girdle, Type 2f
Muscular Dystrophy, Limb-Girdle, Type 2g
Muscular Dystrophy, Limb-Girdle, Type 2h
Muscular Dystrophy, Limb-Girdle, Type 2j
Muscular Dystrophy, Limb-Girdle, Type 2l
Muscular Dystrophy, Limb-Girdle, Type 2q
Muscular Dystrophy, Limb-Girdle, Type 2r
Muscular Dystrophy, Limb-Girdle, Type 2w
Muscular Dystrophy, Limb-Girdle, Type 2x
Muscular Dystrophy, Limb-Girdle, Type 2z
Muscular Dystrophy, Mabry Type
Muscular Dystrophy, Progressive Pectorodorsal
Muscular Dystrophy, Pseudohypertrophic, with Internalized Capillaries
Muscular Dystrophy, Scapulohumeral
Muscular Dystrophy White Matter Spongiosis
Muscular Fibrosis Multifocal Obstructed Vessels
Muscular Hypertonia, Lethal
Muscular Hypertrophy-Hepatomegaly-Polyhydramnios Syndrome
Muscular Hypoplasia, Congenital Universal, of Krabbe
Muscular Phosphorylase Kinase Deficiency
Muscular Pseudohypertrophy-Hypothyroidism Syndrome
Musculocontractural Ehlers-Danlos Syndrome
Musculoskeletal System Benign Neoplasm
Myoclonic Epilepsy Associated with Ragged-Red Fibers
Myofascial Pain Syndrome
Myofibrillar Myopathy
Myoglobinuria
Myoglobinuria, Acute Recurrent, Autosomal Recessive
Myoglobinuria, Autosomal Dominant
Myoglobinuria Dominant Form
Myoglobinuria, Recurrent
Myopathy
Myopathy, Centronuclear, 1
Myopathy, Centronuclear, 2
Myopathy, Centronuclear, 3
Myopathy, Centronuclear, 4
Myopathy, Centronuclear, 5
Myopathy, Congenital
Myopathy, Congenital, Compton-North
Myopathy Due to Malate-Aspartate Shuttle Defect
Myopathy, Lactic Acidosis, and Sideroblastic Anemia
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 1
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 2
Myopathy, Lactic Acidosis, and Sideroblastic Anemia 3
Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay
Myopathy, Myofibrillar, 1
Myopathy, Myofibrillar, 2
Myopathy, Myofibrillar, 3
Myopathy, Myofibrillar, 4
Myopathy, Myofibrillar, 5
Myopathy, Myofibrillar, 6
Myopathy, Myofibrillar, 7
Myopathy, Myofibrillar, 8
Myopathy of Extraocular Muscle
Myopathy, Spheroid Body
Myopathy, Tubular Aggregate, 1
Myopathy, Tubular Aggregate, 2
Myopathy, X-Linked, with Excessive Autophagy
Myopathy, X-Linked, with Postural Muscle Atrophy
Myositis
Myositis Fibrosa
Myositis Ossificans
Myostatin-Related Muscle Hypertrophy
Myotonia Congenita
Myotonia Congenita, Autosomal Dominant
Myotonia Congenita, Autosomal Recessive
Myotonic Disease
Myotonic Dystrophy
Myotonic Dystrophy 1
Myotonic Dystrophy 2
Necrotizing Autoimmune Myopathy
Nemaline Myopathy
Nemaline Myopathy 1
Nemaline Myopathy 10
Nemaline Myopathy 11, Autosomal Recessive
Nemaline Myopathy 2
Nemaline Myopathy 3
Nemaline Myopathy 4
Nemaline Myopathy 5
Nemaline Myopathy 6
Nemaline Myopathy 7
Nemaline Myopathy 8
Nemaline Myopathy 9
Neuronopathy, Distal Hereditary Motor, Type I
Neuronopathy, Distal Hereditary Motor, Type Iia
Neuronopathy, Distal Hereditary Motor, Type Iib
Neuronopathy, Distal Hereditary Motor, Type Iic
Neuronopathy, Distal Hereditary Motor, Type Iid
Neuronopathy, Distal Hereditary Motor, Type Ix
Neuronopathy, Distal Hereditary Motor, Type Va
Neuronopathy, Distal Hereditary Motor, Type Vb
Neuronopathy, Distal Hereditary Motor, Type Viia
Neuronopathy, Distal Hereditary Motor, Type Viib
Neuronopathy, Distal Hereditary Motor, Type Viii
Neuropathy, Hereditary Motor and Sensory, Type Via
Neuropathy, Hereditary Motor and Sensory, Type Vib
Nodular Nonsuppurative Panniculitis
Ocular Muscular Dystrophy
Oculopharyngeal Muscular Dystrophy
Ophthalmoplegic Muscular Dystrophy
Ossification of the Posterior Longitudinal Ligament of Spine
Panniculitis
Patellar Tendinitis
Pigmented Villonodular Synovitis
Poikiloderma, Hereditary Fibrosing, with Tendon Contractures, Myopathy, and Pulmonary Fibrosis
Pontocerebellar Hypoplasia
Pontocerebellar Hypoplasia Type 1
Pontocerebellar Hypoplasia, Type 10
Pontocerebellar Hypoplasia, Type 11
Pontocerebellar Hypoplasia, Type 1a
Pontocerebellar Hypoplasia, Type 1b
Pontocerebellar Hypoplasia, Type 1c
Pontocerebellar Hypoplasia, Type 2a
Pontocerebellar Hypoplasia, Type 2b
Pontocerebellar Hypoplasia, Type 2c
Pontocerebellar Hypoplasia, Type 2d
Pontocerebellar Hypoplasia, Type 2e
Pontocerebellar Hypoplasia, Type 2f
Pontocerebellar Hypoplasia, Type 3
Pontocerebellar Hypoplasia, Type 4
Pontocerebellar Hypoplasia, Type 5
Pontocerebellar Hypoplasia, Type 6
Pontocerebellar Hypoplasia, Type 7
Pontocerebellar Hypoplasia, Type 8
Pontocerebellar Hypoplasia, Type 9
Postpoliomyelitis Syndrome
Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures
Progressive Muscular Atrophy
Proximal Spinal Muscular Atrophy
Puerto Rican Infant Hypotonia Syndrome
Pyomyositis
Qazi Markouizos Syndrome
Reducing Body Myopathy
Rigid Spine Muscular Dystrophy 1
Rippling Muscle Disease 1
Rippling Muscle Disease 2
Round Ligament Malignant Neoplasm
Salih Myopathy
Scapuloperoneal Myopathy
Scapuloperoneal Myopathy, Myh7-Related
Scapuloperoneal Myopathy, X-Linked Dominant
Scapuloperoneal Spinal Muscular Atrophy
Severe Congenital Nemaline Myopathy
Singleton-Merten Syndrome
Singleton-Merten Syndrome 1
Singleton-Merten Syndrome 2
Spinal and Bulbar Muscular Atrophy, X-Linked 1
Spinal Atrophy Ophthalmoplegia Pyramidal Syndrome
Spinal Muscular Atrophy
Spinal Muscular Atrophy-Dandy-Walker Malformation-Cataracts Syndrome
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 2
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 5
Spinal Muscular Atrophy, Distal, X-Linked 3
Spinal Muscular Atrophy, Facioscapulohumeral Type
Spinal Muscular Atrophy, Jokela Type
Spinal Muscular Atrophy, Late-Onset, Finkel Type
Spinal Muscular Atrophy, Lower Extremity-Predominant, 1, Autosomal Dominant
Spinal Muscular Atrophy, Lower Extremity-Predominant, 2, Autosomal Dominant
Spinal Muscular Atrophy, Ryukyuan Type
Spinal Muscular Atrophy, Segmental
Spinal Muscular Atrophy, Type I
Spinal Muscular Atrophy, Type Ii
Spinal Muscular Atrophy, Type Iii
Spinal Muscular Atrophy, Type Iv
Spinal Muscular Atrophy, Type I, with Congenital Bone Fractures
Spinal Muscular Atrophy with Congenital Bone Fractures 2
Spinal Muscular Atrophy with Mental Retardation
Spinal Muscular Atrophy with Microcephaly and Mental Subnormality
Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy
Spinal Muscular Atrophy with Respiratory Distress Type 2
Spinal Muscular Atrophy, X-Linked 2
Superior Transverse Scapular Ligament, Calcification of, Familial
Survival Motor Neuron Spinal Muscular Atrophy
Symptomatic Form of Muscular Dystrophy of Duchenne and Becker in Female Carriers
Temporal Arteritis
Tendinitis
Tendons, Extensor, of Fingers, Anomalous Insertion of
Tendon Sheath Lipoma
Tenosynovial Giant Cell Tumor
Tenosynovitis
Tenosynovitis of Foot and Ankle
Tibial Collateral Ligament Bursitis
Tibialis Tendinitis
Tibial Muscular Dystrophy
Tibial Muscular Dystrophy, Tardive
Torsion Dystonia 17
Torsion Dystonia 2
Torsion Dystonia 4
Torsion Dystonia with Onset in Infancy
Torticollis
Torticollis, Familial
Total Internal Ophthalmoplegia
Ullrich Congenital Muscular Dystrophy 1
Ullrich Congenital Muscular Dystrophy 2
Uterine Ligament Adenocarcinoma
Uterine Ligament Cancer
Uterine Ligament Clear Cell Adenocarcinoma
Uterine Ligament Endometrioid Adenocarcinoma
Uterine Ligament Mucinous Adenocarcinoma
Uterine Ligament Papillary Cystadenoma
Uterine Ligament Serous Adenocarcinoma
Vacuolar Neuromyopathy
Viral Myositis
Visceral Myopathy, Familial, with External Ophthalmoplegia
Walker-Warburg Syndrome
Welander Distal Myopathy
X-Linked Charcot-Marie-Tooth Disease |
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