| Diseases |
Alias |
|
| Spastic Paraplegia 75, Autosomal Recessive |
|
SPG75
|
Hereditary Spastic Paraplegia 75
|
|
Autosomal Recessive Spastic Paraplegia Type 75
|
Autosomal Recessive Spastic Paraplegia 75
|
|
|
| Polyneuropathy |
|
|
| Optic Neuritis |
|
Inflammatory Optic Neuropathy
|
|
|
| Chronic Polyneuropathy |
|
|
| Pelizaeus-Merzbacher Disease |
|
PMD
|
HLD1
|
|
Pelizaeus-Merzbacher Brain Sclerosis
|
Leukodystrophy, Hypomyelinating, 1
|
|
Diffuse Familial Brain Sclerosis
|
Pelizaeus Merzbacher Brain Sclerosis
|
|
Sudanophilic Leukodystrophy, Paelizeus-Merzbacher Type
|
Cockayne-Pelizaeus-Merzbacher Disease
|
|
Hypomyelinating Leukodystrophy 1
|
Leukodystrophy, Sudanophilic
|
|
Pelizaeus Merzbacher Disease
|
Hypomyelinating Leukodystrophy, 1
|
|
Sudanophilic Leukodystrophy
|
Pelizaeus-Merzbacher Disease, Connatal Form
|
|
Connatal Pmd
|
Pelizaeus-Merzbacher Disease Type Ii
|
|
Severe Pmd
|
Null Syndrome
|
|
Plp1 Null Syndrome
|
Pelizaeus-Merzbacher Disease, Null Syndrome
|
|
Brain Sclerosis Diffuse Familial
|
Sudanophilic Leukodystrophy Paelizeus-Merzbacher Type
|
|
Leukodystrophy Hypomyelinating 1
|
Diffuse Cerebral Sclerosis Of Schilder
|
|
|
| Osteosclerotic Myeloma |
|
|
| Kearns-Sayre Syndrome |
|
Ophthalmoplegia
|
Mitochondrial Cytopathy
|
|
KSS
|
Ophthalmoplegia, Pigmentary Degeneration Of Retina, And Cardiomyopathy
|
|
Oculocraniosomatic Syndrome
|
Chronic Progressive External Ophthalmoplegia With Myopathy
|
|
Cpeo With Myopathy
|
Total Ophthalmoplegia
|
|
Ophthalmoplegia-Plus Syndrome
|
Ophthalmoplegia, Progressive External, With Ragged-Red Fibers
|
|
Cpeo With Ragged-Red Fibers
|
Oculomotor Paralysis
|
|
Renal Tubulopathy, Diabetes Mellitus, And Cerebellar Ataxia Due To Duplication O
|
Renal Tubulopathy, Diabetes Mellitus, And Cerebellar Ataxia Due To Duplication Of Mitochondrial Dna
|
|
Proximal Tubulopathy, Diabetes Mellitus And Cerebellar Ataxia
|
Cpeo With Ragged Red Fibers
|
|
Ophthalmoplegia Plus Syndrome
|
Ophthalmoplegia, Progressive External, With Ragged Red Fibers
|
|
Kearns-Sayre Mitochondrial Cytopathy
|
Mitochondrial Myopathies
|
|
|
| Neurofibroma |
|
Neurofibromas
|
Neurofibromatoses
|
|
Nerve Sheath Tumors
|
|
|
| Autoimmune Peripheral Neuropathy |
|
|
| Sensory Peripheral Neuropathy |
|
Sensory Neuropathy
|
Peripheral Sensory Neuropathy
|
|
Hereditary Sensory And Autonomic Neuropathies
|
|
|
| Waldenstroem'S Macroglobulinemia |
|
Waldenstrom Macroglobulinemia
|
Macroglobulinemia Of Waldenstrom
|
|
Waldenström Macroglobulinemia
|
Lymphoplasmacytic Lymphoma With Igm Gammopathy
|
|
Lymphoplasmacytic Lymphoma
|
Waldenstrom'S Macroglobulinaemia
|
|
Waldenstrom'S Syndrome
|
Waldenstrom'S Macroglobulinemia
|
|
Wm
|
Waldenström'S Macroglobulinemia
|
|
Malignant Lymphoma - Lymphoplasmacytic
|
|
|
| Demyelinating Polyneuropathy |
|
Peripheral Demyelinating Neuropathy
|
Demyelinating Peripheral Neuropathy
|
|
|
| Niemann-Pick Disease, Type A |
|
Niemann-Pick Disease Type A
|
Sphingomyelin Lipidosis
|
|
Sphingomyelinase Deficiency
|
Niemann-Pick Disease, Intermediate, Protracted Neurovisceral
|
|
Acid Sphingomyelinase Deficiency, Neurovisceral Type
|
Asmd, Neurovisceral Type
|
|
Infantile Neurovisceral Acid Sphingomyelinase Deficiency
|
Infantile Neurovisceral Asmd
|
|
Npd-A
|
Niemann-Pick Disease A
|
|
NPDA
|
Classical Niemann-Pick Disease
|
|
Niemann-Pick Disease Acute Neuronopathic Form
|
Niemann-Pick Disease Acute Neurovisceral Form
|
|
Niemann-Pick Disease Classical Infantile Form
|
Niemann-Pick Disease Intermediate Protracted Neurovisceral
|
|
Niemann-Pick Disease Neuronopathic Type
|
Niemann-Pick Disease Type I
|
|
Npa
|
Niemann-Pick Diseases
|
|
|
| Neuritis |
|
|
| Autoimmune Neuropathy |
|
|
| Asymmetric Motor Neuropathy |
|
|
| Miller Fisher Syndrome |
|
Cranial Variant Of Gbs
|
Fisher'S Syndrome
|
|
Miller-Fisher Variant Of Guillain-Barre Syndrome
|
Miller-Fisher Syndrome
|
|
Cranial Variant Of Guillain-Barré Syndrome
|
Cranial Variant Of Guillain-Barre Syndrome
|
|
Fisher Syndrome
|
|
|
| Multiple Sclerosis |
|
MS
|
Multiple Sclerosis, Susceptibility To
|
|
Disseminated Sclerosis
|
Multiple Sclerosis, Disease Progression, Modifier Of
|
|
Insular Sclerosis
|
Multiple Sclerosis Modifier Of Disease Progression
|
|
Multiple Sclerosis, Susceptibility To 1
|
Multiple Sclerosis, Susceptibility To, 1
|
|
Multiple Sclerosis 1
|
Generalized Multiple Sclerosis
|
|
Multiple Sclerosis Variant
|
Multiple Sclerosis Susceptibility To
|
|
Cerebrospinal Sclerosis
|
Generalised Multiple Sclerosis
|
|
Ms - [Multiple Sclerosis]
|
Disseminated Cerebrospinal Sclerosis
|
|
Disseminated Multiple Sclerosis
|
Disseminated Nervous System Myelosclerosis
|
|
Multiple Cerebrospinal Sclerosis
|
Multiple Combined Sclerosis
|
|
Multiple Sclerosis Generalised
|
Disseminated Brain Sclerosis
|
|
Disseminated Spinal Sclerosis
|
Insular Brain Sclerosis
|
|
Miliary Brain Sclerosis
|
Multiple Combined Sclerosis Of Spinal Cord
|
|
Multiple Ascending Sclerosis
|
Multiple Brain Sclerosis
|
|
Multiple Sclerosis Of Brain Stem
|
Multiple Sclerosis Of The Brain Stem
|
|
Multiple Sclerosis Of Cord
|
Sclérose En Plaques
|
|
Plaque Sclerosis
|
Multiple Sclerosis Of The Spinal Cord
|
|
|
| Demyelinating Disease |
|
Demyelinating Diseases
|
Demyelinating Disorder
|
|
|
| Niemann-Pick Disease |
|
Sphingomyelin/Cholesterol Lipidosis
|
Niemann-Pick Diseases
|
|
Lipoid Histiocytosis
|
Sphingomyelin Lipidosis
|
|
Sphingomyelinase Deficiency Disease
|
Lipid Histiocytosis
|
|
Neuronal Cholesterol Lipidosis
|
Neuronal Lipidosis
|
|
Npd
|
Sphingomyelinase Deficiency
|
|
Niemann-Pick Disease, Type A
|
|
|
| Chronic Inflammatory Demyelinating Polyradiculoneuropathy |
|
Chronic Inflammatory Demyelinating Polyneuropathy
|
Cidp
|
|
Polyradiculoneuropathy Chronic Inflammatory Demyelinating
|
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
|
|
|
| Polyradiculopathy |
|
|
| Autoimmune Disease Of Peripheral Nervous System |
|
|
| Mononeuropathy |
|
|
| Autoimmune Optic Neuritis |
|
|
| Mononeuritis Multiplex |
|
|
| Plexopathy |
|
|
| Balo Concentric Sclerosis |
|
Balo'S Concentric Sclerosis
|
Balo Disease
|
|
Diffuse Cerebral Sclerosis Of Schilder
|
Tumefactive Multiple Sclerosis
|
|
Concentric Demyelination
|
Balo'S Disease
|
|
Baló Concentric Sclerosis
|
Encephalitis Periaxialis Concentrica
|
|
Marburg Variant
|
|
|
| Hereditary Neuropathies |
|
|
| Motor Peripheral Neuropathy |
|
Motor Neuritis
|
Peripheral Motor Neuropathy
|
|
Hereditary Motor And Sensory Neuropathy
|
Hsmn
|
|
Hsmn - Hereditary Sensory And Motor Neuropathy
|
Neuropathic Muscular Atrophy
|
|
Hereditary Sensory And Motor Neuropathy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Mononeuritis Of Upper Limb And Mononeuritis Multiplex |
|
|
| Monoclonal Gammopathy Of Uncertain Significance |
|
Monoclonal Gammopathy Of Undetermined Significance
|
Mgus
|
|
Mgus - [Monoclonal Gammopathy Of Undetermined Significance]
|
Monoclonal Gammopathy Nos
|
|
Iga Gammopathy
|
Monoclonal Gammoglobulinopathy
|
|
|
| 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
|
Bulbar Syndrome
|
|
Anterior Horn Cell Disorder
|
Hereditary Motor Neuron Disease
|
|
|
| Neuropathy, Hereditary, With Liability To Pressure Palsies |
|
Tomaculous Neuropathy
|
Hereditary Neuropathy With Liability To Pressure Palsies
|
|
HNPP
|
Polyneuropathy, Familial Recurrent
|
|
Neuropathy, Recurrent, With Pressure Palsies
|
Current Pressure-Sensitive Neuropathy
|
|
Familial Recurrent Polyneuropathy
|
Heterozygous Microdeletion 17p11.2p12
|
|
Potato-Grubbing Palsy
|
Tulip-Bulb Digger'S Palsy
|
|
Compression Neuropathy
|
Entrapment Neuropathy
|
|
Familial Pressure Sensitive Neuropathy
|
Hereditary Motor And Sensory Neuropathy
|
|
Hereditary Pressure Sensitive Neuropathy
|
Inherited Tendency To Pressure Palsies
|
|
Hereditary Liability To Pressure Palsies
|
Nerve Compression Syndrome
|
|
Entrapment Neuropathies
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Blood Protein Disease |
|
Blood Protein Disorders
|
Blood Protein Disorder
|
|
|
| Cerebral Lymphoma |
|
Primary Cerebral Lymphoma
|
Brain Primary Lymphoma
|
|
Primary Lymphoma Of Cerebrum
|
|
|
| Charcot-Marie-Tooth Disease And Deafness |
|
Charcot-Marie-Tooth Disease Type 1e
|
CMT1E
|
|
Charcot-Marie-Tooth Disease Type 1
|
Hereditary Motor And Sensory Neuropathy Type 1
|
|
Charcot-Marie-Tooth Disease, Demyelinating, Type 1e
|
Charcot-Marie-Tooth Disease, Type I
|
|
Charcot-Marie-Tooth Neuropathy And Deafness, Autosomal Dominant
|
Charcot-Marie-Tooth Disease, Type 1e
|
|
Charcot-Marie-Tooth Disease Demyelinating Type 1e
|
Autosomal Dominant Demyelinating Charcot-Marie-Tooth Disease
|
|
Cmt1
|
Charcot-Marie-Tooth Neuropathy Type 1
|
|
Autosomal Dominant Charcot-Marie-Tooth Neuropathy And Deafness
|
Charcot-Marie-Tooth Disease-Deafness
|
|
Charcot-Marie-Tooth Type 1
|
Hmsn1
|
|
Hereditary Motor And Sensory Neuropathy 1
|
Cmt 1e
|
|
Charcot Marie Tooth Disease Type 1e
|
Charcot-Marie-Tooth Disease-Deafness Syndrome
|
|
Charcot-Marie-Tooth Disease-Hearing Loss Syndrome
|
Charcot-Marie-Tooth Disease 1e
|
|
Charcot-Marie-Tooth Disease And Deafness Autosomal Dominant
|
Charcot-Marie-Tooth Neuropathy Type 1e
|
|
Charcot-Marie-Tooth Disease, Type Ie
|
Hereditary Motor And Sensory Neuropathy Type I
|
|
|
| Wallerian Degeneration |
|
Wallerian Degeneration Of The Pyramidal Tract
|
|
|
| Central Pontine Myelinolysis |
|
Myelinolysis, Central Pontine
|
Osmotic Demyelination Syndrome
|
|
Cpm
|
Myelinolysis Central Pontine
|
|
Central Pontine Myelinosis
|
|
|
| Acute Disseminated Encephalomyelitis |
|
Acute Disseminated Encephalitis
|
Adem
|
|
Ade
|
Encephalomyelitis Acute Disseminated
|
|
Encephalomyelitis, Acute Disseminated
|
Adem - [Acute Disseminated Encephalomyelitis]
|
|
|
| Hypertrophic Neuropathy Of Dejerine-Sottas |
|
Dejerine-Sottas Disease
|
Dejerine-Sottas Syndrome
|
|
Charcot-Marie-Tooth Disease Type 3
|
DSS
|
|
Hereditary Motor And Sensory Neuropathy Type Iii
|
Hmsn3
|
|
Dejerine-Sottas Neuropathy
|
Hmsn Iii
|
|
Charcot-Marie-Tooth Disease, Type 3
|
Cmt3
|
|
Dsn
|
Hmsn 3
|
|
Hereditary Motor And Sensory Neuropathy Type 3
|
Hereditary Motor And Sensory Neuropathy 3
|
|
Hypertrophic Neuropathy Of Infancy
|
Charcot-Marie-Tooth Disease Demyelinating Type 4f
|
|
Charcot-Marie-Tooth Disease Type 4f
|
Charcot-Marie-Tooth Neuropathy Type 4f
|
|
Cmt4f
|
Hereditary Motor And Sensory Neuropathy Iii
|
|
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
|
|
|
| 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
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Lymphoplasmacytic Lymphoma |
|
Waldenstrom Macroglobulinemia
|
Malignant Lymphoma - Lymphoplasmacytic
|
|
Waldenström Macroglobulinaemia
|
Waldenström Macroglobulinaemia Without Mention Of Remission
|
|
Idiopathic Macroglobulinaemia
|
Primary Macroglobulinaemia
|
|
|
| Progressive Relapsing Multiple Sclerosis |
|
Prms
|
Progressive-Relapsing Ms
|
|
Multiple Sclerosis, Progressive Relapsing
|
|
|
| Charcot-Marie-Tooth Disease, Demyelinating, Type 1a |
|
Charcot-Marie-Tooth Disease Type 1a
|
CMT1A
|
|
Charcot-Marie-Tooth Disease, Type Ia
|
Hmsn1a
|
|
Hereditary Motor And Sensory Neuropathy Ia
|
Hmsn Ia
|
|
Charcot-Marie-Tooth Neuropathy, Type 1a
|
Charcot-Marie-Tooth Disease, Type 1a
|
|
Charcot-Marie-Tooth Neuropathy Type 1a
|
Hereditary Motor And Sensory Neuropathy 1a
|
|
Microduplication 17p12
|
Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1a
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease With Focally Folded Myelin Sheaths Type 1a
|
Cmt 1a
|
|
Charcot Marie Tooth Disease Type 1a
|
Hmsn 1a
|
|
Charcot-Marie-Tooth Disease 1a
|
Charcot-Marie-Tooth Disease Demyelinating Type 1a
|
|
Charcot-Marie-Tooth Disease Slow Nerve Conduction Type Unlinked To Duffy
|
|
|
| Primary Progressive Multiple Sclerosis |
|
Ppms
|
Primary-Progressive Ms
|
|
Multiple Sclerosis, Primary Progressive
|
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Hypomyelinating Leukodystrophy |
|
Hld
|
Leukodystrophy, Hypomyelinating
|
|
|
| Leukodystrophy, Hypomyelinating, 5 |
|
Hypomyelination And Congenital Cataract
|
HLD5
|
|
Hypomyelination-Congenital Cataract Syndrome
|
Hypomyelinating Leukodystrophy 5
|
|
Hcc
|
Hypomyelination And Congenital Cataract: Hcc
|
|
Hypomyelination - Congenital Cataract
|
Hypomyelination With Congenital Cataract
|
|
|
| Plasma Protein Metabolism Disease |
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| Autoimmune Disease Of Central Nervous System |
|
|
| Metachromatic Leukodystrophy |
|
Arylsulfatase A Deficiency
|
MLD
|
|
Arsa Deficiency
|
Sulfatide Lipidosis
|
|
Metachromatic Leukoencephalopathy
|
Cerebral Sclerosis, Diffuse, Metachromatic Form
|
|
Cerebroside Sulfatase Deficiency
|
Leukodystrophy, Metachromatic
|
|
Pseudoarylsulfatase A Deficiency
|
Leukodystrophy Metachromatic
|
|
Sulfatidosis
|
Metachromatic Leukodystrophy, Late Infantile
|
|
Metachromatic Leukodystrophy Variant
|
Deficiency Of Cerebroside-Sulfatase
|
|
Scholz Cerebral Sclerosis
|
Sulfatide Lipoidosis
|
|
Cerebral Sclerosis Diffuse Metachromatic Form
|
Arylsulfatase A Deficiency Disease
|
|
Cerebroside Sulphatase Deficiency Disease
|
Greenfield Disease
|
|
Metachromatic Leukodystrophy, Adult
|
Metachromatic Leukodystrophy, Juvenile
|
|
Leukodystrophy Metachromatic Adult
|
Leukodystrophy Metachromatic Juvenile
|
|
Leukodystrophy Metachromatic Late Infantile
|
Metachromatic Leukodystrophy, Adult Type
|
|
Metachromatic Leukodystrophy, Juvenile Type
|
Metachromatic Leukodystrophy, Infant
|
|
Greenfield'S Disease
|
|
|
| Dystonia |
|
Dystonic Disease
|
Dystonic Disorder
|
|
Dystonia Disorders
|
Neuroleptic Dyskinesia
|
|
|
| Optic Nerve Disease |
|
Optic Neuropathy
|
Disorder Of The Second Nerve
|
|
Optic Nerve Disorder
|
Optic Nerve
|
|
Abnormality Of The Optic Nerve
|
Optic Nerve Disorders
|
|
Neuropathy, Optic
|
Disorder Of The Optic Nerve
|
|
|
| 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
|
|
|
| Myeloma, Multiple |
|
Multiple Myeloma
|
Plasma Cell Myeloma
|
|
Kahler Disease
|
Myelomatosis
|
|
Medullary Plasmacytoma
|
Multiple Myeloma, Resistance To
|
|
Myeloma
|
Plasma Cell Dyscrasia
|
|
Kahler'S Disease
|
Multiple Myeloma, Susceptibility To
|
|
Myeloma - Multiple
|
Kahler-Bozzolo Disease
|
|
Plasma Cell Myelomas
|
MM
|
|
Plasma Cell Neoplasm
|
Primary Systemic Amyloidosis
|
|
Primary Amyloidosis
|
Immunoglobulin Deposition Disease
|
|
Plasmacytic Myeloma
|
Multiple Myelomata
|
|
Multiple Myeloma Nos
|
Multiple Myeloma Without Mention Of Remission
|
|
Monostotic Plasma Cell Myeloma
|
Mm - [Multiple Myeloma]
|
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
| Hereditary Spastic Paraplegia |
|
Familial Spastic Paraplegia
|
Hereditary Spastic Paraparesis
|
|
Strumpell-Lorrain Disease
|
Familial Spastic Paraparesis
|
|
Hsp
|
Spg
|
|
Strümpell-Lorrain Disease
|
Spastic Paraplegia, Hereditary
|
|
French Settlement Disease
|
Strumpell-Lorrain Syndrome
|
|
Fsp
|
Spastic Paraplegia, Familial
|
|
Spastic Paraplegia Hereditary
|
Spastic Paraplegia 3, Autosomal Dominant
|
|
Spastic Paraparesis
|
Hereditary Spastic Paralysis
|
|
Familial Spastic Paralysis
|
Hereditary Spastic Ataxia
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
