Informaţii despre
| Nume | | Hereditary motor and sensory neuropathy |
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| Pagina Web | | apps.who.int |
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| Boli A-Z | | Agenesis of the Corpus Callosum with Peripheral Neuropathy
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 Intermediate Charcot-Marie-Tooth Disease with Neuropathic Pain
Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease and Deafness
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a2a
Charcot-Marie-Tooth Disease, Axonal, Type 2a1
Charcot-Marie-Tooth Disease, Axonal, Type 2b
Charcot-Marie-Tooth Disease, Axonal, Type 2b1
Charcot-Marie-Tooth Disease, Axonal, Type 2b2
Charcot-Marie-Tooth Disease, Axonal, Type 2d
Charcot-Marie-Tooth Disease, Axonal, Type 2e
Charcot-Marie-Tooth Disease, Axonal, Type 2f
Charcot-Marie-Tooth Disease, Axonal, Type 2h
Charcot-Marie-Tooth Disease, Axonal, Type 2i
Charcot-Marie-Tooth Disease, Axonal, Type 2j
Charcot-Marie-Tooth Disease, Axonal, Type 2k
Charcot-Marie-Tooth Disease, Axonal, Type 2l
Charcot-Marie-Tooth Disease, Axonal, Type 2n
Charcot-Marie-Tooth Disease, Axonal, Type 2o
Charcot-Marie-Tooth Disease, Axonal, Type 2p
Charcot-Marie-Tooth Disease, Axonal, Type 2q
Charcot-Marie-Tooth Disease, Axonal, Type 2r
Charcot-Marie-Tooth Disease, Axonal, Type 2t
Charcot-Marie-Tooth Disease, Axonal, Type 2u
Charcot-Marie-Tooth Disease, Axonal, Type 2v
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, Dominant Intermediate D
Charcot-Marie-Tooth Disease, Dominant Intermediate E
Charcot-Marie-Tooth Disease, Dominant Intermediate F
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, Recessive Intermediate D
Charcot-Marie-Tooth Disease Type 2a2
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, 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
Cowchock Syndrome
Dnajb2-Related Charcot-Marie-Tooth Disease Type 2
Facial Onset Sensory and Motor Neuronopathy
Giant Axonal Neuropathy 2, Autosomal Dominant
Hereditary Motor and Sensory Neuropathy, Type Iic
Hereditary Motor and Sensory Neuropathy V
Hereditary Motor and Sensory Neuropathy with Acrodystrophy
Hypertrophic Neuropathy of Dejerine-Sottas
Motor Peripheral Neuropathy
Neuromyotonia and Axonal Neuropathy, Autosomal Recessive
Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive
Neuropathy, Hereditary Motor and Sensory, Okinawa Type
Neuropathy, Hereditary Motor and Sensory, Russe Type
Neuropathy, Hereditary Motor and Sensory, Type Via
Neuropathy, Hereditary Motor and Sensory, with Deafness, Mental Retardation, and Absent Sensory Large Myelinated Fibers
Neuropathy, Hereditary Thermosensitive
Neuropathy, Hereditary, with Liability to Pressure Palsies
Neuropathy, Hereditary, with or Without Age-Related Macular Degeneration
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss
Roussy-Levy Hereditary Areflexic Dystasia
Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency
Slowed Nerve Conduction Velocity, Autosomal Dominant |
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