| 疾病名称 |
别名 |
|
| Spastic Paraplegia 10, Autosomal Dominant |
|
SPG10
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Hereditary Spastic Paraplegia 10
|
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Autosomal Dominant Spastic Paraplegia Type 10
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Spastic Paraplegia 10
|
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Spastic Paraplegia 10 With Or Without Peripheral Neuropathy
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Autosomal Dominant Spastic Paraplegia 10
|
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Autosomal Dominant Spastic Paraplegia
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Spastic Paraplegia, Autosomal Dominant
|
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Paraplegia, Spastic, Autosomal Dominant, Type 10
|
|
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| Myoclonus, Intractable, Neonatal |
|
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| Amyotrophic Lateral Sclerosis 25 |
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Amyotrophic Lateral Sclerosis, Susceptibility To, 25
|
ALS25
|
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Sclerosis, Lateral, Amyotrophic, Type 25
|
|
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| Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Kif5a Mutation |
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Cmt2 Due To Kif5a Mutation
|
|
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| Demyelinating Polyneuropathy |
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Peripheral Demyelinating Neuropathy
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Demyelinating Peripheral Neuropathy
|
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| Hereditary Spastic Paraplegia |
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Familial Spastic Paraplegia
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Hereditary Spastic Paraparesis
|
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Strumpell-Lorrain Disease
|
Familial Spastic Paraparesis
|
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Hsp
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Spg
|
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Strümpell-Lorrain Disease
|
Spastic Paraplegia, Hereditary
|
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French Settlement Disease
|
Strumpell-Lorrain Syndrome
|
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Fsp
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Spastic Paraplegia, Familial
|
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Spastic Paraplegia Hereditary
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Spastic Paraplegia 3, Autosomal Dominant
|
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Spastic Paraparesis
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Hereditary Spastic Paralysis
|
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Familial Spastic Paralysis
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Hereditary Spastic Ataxia
|
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| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 4 |
|
FTDALS4
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Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-4
|
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Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 4
|
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| Paraplegia |
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Paraplegia, Lower
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Severe Or Complete Loss Of Motor Function In The Lower Extremities And Lower Portions Of The Trunk
|
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| Charcot-Marie-Tooth Disease, Axonal, Type 2e |
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Charcot-Marie-Tooth Disease Type 2
|
CMT2E
|
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CMT2S
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CMT2Y
|
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Charcot-Marie-Tooth Disease Type 2e
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Charcot-Marie-Tooth Disease Type 2y
|
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Charcot-Marie-Tooth Disease Axonal Type 2s
|
Charcot-Marie-Tooth Disease, Axonal, Type 2s
|
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Charcot-Marie-Tooth Disease, Type 2e
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Hereditary Motor And Sensory Neuropathy Type 2
|
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Charcot-Marie-Tooth Neuropathy, Type 2s
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Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2s
|
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Charcot-Marie-Tooth Disease, Axonal, Type 2y
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Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2y
|
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Charcot-Marie-Tooth Neuropathy, Type 2y
|
Charcot-Marie-Tooth Disease, Type 2y
|
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Autosomal Dominant Charcot-Marie-Tooth Disease Type 2e
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Charcot-Marie-Tooth Neuropathy Type 2e
|
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Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Vcp Mutation
|
Cmt2 Due To Vcp Mutation
|
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Charcot-Marie-Tooth Disease Type 2s
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Autosomal Dominant Charcot-Marie-Tooth Disease Type 2
|
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Autosomal Dominant Axonal Charcot-Marie-Tooth Disease
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Cmt2
|
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Charcot-Marie-Tooth Neuropathy, Type 2e
|
Hereditary Motor And Sensory Neuropathy Guadalajara Neuronal Type
|
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Hereditary Motor And Sensory Neuropathy Okinawa Type
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Autosomal Dominant Axonal Charcot-Marie-Tooth Type 2y
|
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Charcot-Marie-Tooth Neuropathy Type 2y
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Autosomal Recessive Axonal Charcot-Marie-Tooth Type 2s
|
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Charcot-Marie-Tooth Neuropathy Type 2s
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Charcot-Marie-Tooth Type 2
|
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Autosomal Dominant Charcot-Marie-Tooth Disease Type 2y
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Charcot-Marie-Tooth Disease 2e
|
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Charcot-Marie-Tooth Disease Axonal Type 2e
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Charcot-Marie-Tooth Disease Neuronal Type 2e
|
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Charcot-Marie-Tooth Disease 2s
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Charcot-Marie-Tooth Neuropathy Axonal Type 2s
|
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Charcot-Marie-Tooth Disease 2y
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Charcot-Marie-Tooth Disease, Type 2
|
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Hereditary Motor And Sensory-Neuropathy Type Ii
|
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| Peripheral Nervous System Disease |
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Peripheral Neuropathy
|
Peripheral Nerve Disease
|
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Peripheral Nerve Disorders
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Neuropathy, Peripheral
|
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Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
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| Nescav Syndrome |
|
NESCAVS
|
Neurodegeneration And Spasticity With Or Without Cerebellar Atrophy Or Cortical Visual Impairment
|
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Mrd9
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Intellectual Disability, Autosomal Dominant 9
|
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Mental Retardation, Autosomal Dominant 9, Formerly
|
Mrd9, Formerly
|
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Autosomal Dominant Intellectual Disability 9
|
Autosomal Dominant Non-Syndromic Intellectual Disability 9
|
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Mental Retardation, Autosomal Dominant 9
|
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| Lateral Sclerosis |
|
Primary Lateral Sclerosis
|
Adult-Onset Primary Lateral Sclerosis
|
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Adult-Onset Pls
|
Motor Neuron Disease
|
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Pls
|
Pls - [Primary Lateral Sclerosis]
|
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Lateral Spinal Sclerosis
|
Lateral Complete Paralysis
|
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Lateral Incomplete Paralysis
|
Lateral Paralysis
|
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| Hereditary Spastic Paraplegia 30 |
|
Autosomal Spastic Paraplegia Type 30
|
Spg30
|
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Autosomal Recessive Spastic Paraplegia 30
|
|
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| Asbestosis |
|
Idiopathic Interstitial Pneumonitis - From Asbestos Exposure
|
Pulmonary Fibrosis - From Asbestos Exposure
|
|
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| Neuropathy, Hereditary Sensory, Type Id |
|
HSN1D
|
Hereditary Sensory Neuropathy Type 1d
|
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Neuropathy, Hereditary Sensory, Type 1d
|
Neuropathy, Hereditary Sensory, 1d
|
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Hereditary Sensory Neuropathy Type Id
|
Neuropathy, Sensory, Hereditary, Type Id
|
|
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| Neuropathy, Hereditary Sensory, Type Iic |
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HSN2C
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Hereditary Sensory Neuropathy Type 2c
|
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Hereditary Sensory Neuropathy Type Iic
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Neuropathy, Hereditary Sensory, Type 2c
|
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Neuropathy, Hereditary Sensory, 2c
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Hsn Iice
|
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Neuropathy, Sensory, Hereditary, Type Iic
|
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| Motor Peripheral Neuropathy |
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Motor Neuritis
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Peripheral Motor Neuropathy
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Hereditary Motor And Sensory Neuropathy
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Hsmn
|
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Hsmn - Hereditary Sensory And Motor Neuropathy
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Neuropathic Muscular Atrophy
|
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Hereditary Sensory And Motor Neuropathy
|
Hereditary Motor And Sensory Neuropathies
|
|
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| Spastic Paraplegia 13, Autosomal Dominant |
|
SPG13
|
Hereditary Spastic Paraplegia 13
|
|
Autosomal Dominant Spastic Paraplegia 13
|
Spastic Paraplegia 13
|
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Autosomal Dominant Spastic Paraplegia Type 13
|
Spastic Paraplegia-13
|
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Paraplegia, Spastic, Type 13
|
|
|
| Spastic Paraplegia 2, X-Linked |
|
SPG2
|
Hereditary Spastic Paraplegia 2
|
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Sppx2
|
Spastic Paraplegia Type 2
|
|
Spastic Paraplegia 2
|
Hereditary X-Linked Recessive Spastic Paraplegia
|
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X-Linked Spastic Paraplegia 2
|
X Linked Recessive Hereditary Spastic Paraplegia
|
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Spastic Gait Type 2
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Spastic Paraparesis Type 2
|
|
X-Linked Spastic Paraplegia Type 2
|
Spastic Paraplegia Type 2, X-Linked
|
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Spastic Paraplegia-2
|
Paraplegia, Spastic, Type 2
|
|
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| Spastic Paraplegia 75, Autosomal Recessive |
|
SPG75
|
Hereditary Spastic Paraplegia 75
|
|
Autosomal Recessive Spastic Paraplegia Type 75
|
Autosomal Recessive Spastic Paraplegia 75
|
|
|
| Masa Syndrome |
|
L1 Syndrome
|
Crash Syndrome
|
|
X-Linked Hydrocephalus Syndrome
|
SPG1
|
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Gareis-Mason Syndrome
|
Spastic Paraplegia 1, X-Linked
|
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Corpus Callosum Hypoplasia-Retardation-Adducted Thumbs-Spasticity-Hydrocephalus Syndrome
|
L1cam Syndrome
|
|
Spastic Paraplegia 1
|
Mental Retardation, Aphasia, Shuffling Gait, And Adducted Thumbs
|
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Clasped Thumb And Mental Retardation
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Thumb, Congenital Clasped, With Mental Retardation
|
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Adducted Thumb With Mental Retardation
|
Hereditary Spastic Paraplegia 1
|
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X-Linked Complicated Hereditary Spastic Paraplegia Type 1
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X-Linked Corpus Callosum Agenesis
|
|
X-Linked Spastic Paraplegia 1
|
L1 Disease
|
|
X-Linked Intellectual Disability - Corpus Callosum Agenesis - Spastic Quadriparesis
|
Adducted Thumb With Intellectual Disability
|
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Clasped Thumb And Intellectual Disability
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Intellectual Disability Aphasia Shuffling Gait Adducted Thumbs
|
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Thumb Congenital Clasped With Intellectual Disability
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X-Linked Intellectual Disability-Corpus Callosum Agenesis-Spastic Quadriparesis Syndrome
|
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Adducted Thumbs-Mental Retardation Syndrome
|
Corpus Callosum Hypoplasia, Mental Retardation, Adducted Thumbs, Spastic Paraplegia, Hydrocephalus Syndrome
|
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Mental Retardation-Clasped Thumb Syndrome
|
Intellectual Disability-Aphasia-Shuffling Gait-Adducted Thumbs Syndrome
|
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Spastic Paraplegia Type 1, X-Linked
|
MASA
|
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Corpus Callosum Hypoplasia-Psychomotor Retardation, Adducted Thumbs-Spastic Paraparesis-Hydrocephalus
|
Crash
|
|
Masa Syndrome
|
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| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
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Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Amyotrophic Lateral Sclerosis 9 |
|
Amyotrophic Lateral Sclerosis Type 9
|
ALS9
|
|
Sclerosis, Lateral, Amyotrophic, Type Type 9
|
|
|
| Pseudobulbar Palsy |
|
|
| Spastic Paraplegia 42, Autosomal Dominant |
|
SPG42
|
Hereditary Spastic Paraplegia 42
|
|
Autosomal Dominant Spastic Paraplegia Type 42
|
Autosomal Dominant Spastic Paraplegia 42
|
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Paraplegia, Spastic, Type 42, Autosomal Dominant
|
|
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| Neuronopathy, Distal Hereditary Motor, Type Viib |
|
HMN7B
|
Hmn Viib
|
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Dhmn7b
|
Neuropathy, Distal Hereditary Motor, Type Viib
|
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Distal Hereditary Motor Neuronopathy Type 7b
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Distal Hereditary Motor Neuropathy Type Viib
|
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Neuronopathy, Distal Hereditary Motor, Type 7b
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Neuropathy, Distal Hereditary Motor, With Vocal Cord Paralysis, Type Viib
|
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Lower Motor Neuron Disease, Dynactin Type
|
Distal Spinal Muscular Atrophy With Vocal Cord Paralysis Type 7b
|
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Harper-Young Myopathy
|
Neuronopathy, Distal Hereditary Motor, 7b
|
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Distal Hereditary Motor Neuropathy With Vocal Cord Paralysis Type Viib
|
Lower Motor Neuron Disease Dynactin Type
|
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Plmnd
|
Progressive Lower Motor Neuron Disease
|
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Neuropathy, Motor, Distal, Hereditary, Type Viib
|
|
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| Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive |
|
Charcot-Marie-Tooth Disease Type 4
|
Charcot-Marie-Tooth Disease Type 4e
|
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Hereditary Motor And Sensory Neuropathy
|
Cmt4e
|
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CHN1
|
Hypomyelinating Neuropathy, Congenital, 1
|
|
Charcot-Marie-Tooth Neuropathy Type 4e
|
Neuropathy, Congenital Hypomyelinating, 1
|
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Ar-Cmt1
|
Autosomal Recessive Demyelinating Charcot-Marie-Tooth
|
|
Cmt4
|
Neuropathy, Congenital Hypomyelinating Or Amyelinating, Autosomal Recessive
|
|
Hypomyelination, Severe Congenital
|
Charcot-Marie-Tooth Disease, Type 4e
|
|
Charcot-Marie-Tooth Neuropathy, Type 4e
|
Autosomal Recessive Congenital Hypomyelinating Or Amyelinating Neuropathy
|
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Autosomal Recessive Congenital Hypomyelinating Neuropathy
|
Congenital Amyelinating Neuropathy
|
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Congenital Hypomyelinating Neuropathy Autosomal Recessive
|
Neuropathy, Congenital Hypomyelinating Or Amyelinating
|
|
Severe Congenital Hypomyelination
|
Hereditary Sensory Motor Neuropathy
|
|
Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive
|
Neuropathy, Hypomyelinating, Congenital, Type 1
|
|
Neuropathy, Motor And Sensory, Hereditary
|
Congenital Hypomyelinating Neuropathy
|
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Hereditary Motor And Sensory Neuropathies
|
Hereditary Sensorimotor Neuropathy
|
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Hmsn - [Hereditary Motor And Sensory Neuropathy]
|
Hsmn - [Hereditary Sensory And Motor Neuropathy]
|
|
Hereditary Motor And Sensory Neuropathy, Types I-Iv
|
|
|
| Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1 |
|
FTDALS1
|
Frontotemporal Dementia And/Or Motor Neuron Disease
|
|
Ftdmnd
|
Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia
|
|
Alsftd
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis
|
|
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-1
|
Frontotemporal Dementia With Motor Neuron Disease
|
|
Ftdals
|
Ftd-Als
|
|
Ftd-Mnd
|
Frontotemporal Dementia With Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis With Frontotemporal Dementia 1
|
Amyotrophic Lateral Sclerosis/Frontotemporal Dementia
|
|
Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis
|
Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia 1
|
|
Frontotemporal Lobar Degeneration
|
Grn-Related Frontotemporal Dementia
|
|
|
| Spastic Paraplegia 17, Autosomal Dominant |
|
Silver Syndrome
|
SPG17
|
|
Silver Spastic Paraplegia Syndrome
|
Spastic Paraplegia With Amyotrophy Of Hands And Feet
|
|
Hereditary Spastic Paraplegia 17
|
Autosomal Dominant Spastic Paraplegia Type 17
|
|
Spastic Paraplegia 17
|
Spastic Paraplegia-Amyotrophy Of Hands And Feet
|
|
Autosomal Dominant Spastic Paraplegia 17
|
Dhmn5b
|
|
Distal Hereditary Motor Neuropathy Type 5b
|
Paraplegia, Spastic, Autosomal Dominant, Type 17
|
|
Russell-Silver Syndrome
|
Neuronopathy, Distal Hereditary Motor, Type Vb
|
|
|
| Spastic Ataxia |
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
| Amyotrophic Lateral Sclerosis 1 |
|
Amyotrophic Lateral Sclerosis
|
ALS
|
|
Lou Gehrig Disease
|
Amyotrophic Lateral Sclerosis Type 1
|
|
Charcot Disease
|
ALS1
|
|
Amyotrophic Lateral Sclerosis, Susceptibility To
|
Fals
|
|
Lou Gehrig'S Disease
|
Mnd
|
|
Motor Neuron Disease
|
Familial Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis 1, Familial
|
Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
|
|
Motor Neuron Disease, Bulbar
|
Motor Neurone Disease
|
|
Amyotrophic Lateral Sclerosis With Dementia
|
Dementia With Amyotrophic Lateral Sclerosis
|
|
Motor Neuron Disease, Amyotrophic Lateral Sclerosis
|
Sclerosis, Lateral, Amyotrophic
|
|
Sclerosis, Lateral, Amyotrophic, Type 1
|
Amyotrophic Sclerosis
|
|
Als - [Amyotrophic Lateral Sclerosis]
|
Wasting Palsy
|
|
Amyotrophic Paralysis
|
Amyotrophy Lateral Sclerosis
|
|
Wasting Paralysis
|
Spinal Progressive Amyotrophy
|
|
Progressive Atrophic Paralysis
|
|
|
