| Diseases |
Alias |
|
| Myasthenic Syndrome, Congenital, 8 |
|
Congenital Myasthenic Syndrome 8
|
CMS8
|
|
Myasthenic Syndrome, Congenital, With Pre- And Postsynaptic Defects
|
Cmsppd
|
|
Myasthenic Syndrome, Congenital, 8, With Pre- And Postsynaptic Defects
|
Congenital Myasthenic Syndrome Due To Agrin Deficiency
|
|
Myasthenic Syndrome, Congenital, Due To Agrin Deficiency
|
Congenital Myasthenic Syndrome 8 With Pre- And Postsynaptic Defects
|
|
Myasthenic Syndrome, Congenital, Type 8, With Pre- And Postsynaptic Defects
|
|
|
| Presynaptic Congenital Myasthenic Syndromes |
|
Presynaptic Congenital Myasthenic Syndrome
|
Congenital Myasthenic Syndromes, Presynaptic
|
|
|
| Postsynaptic Congenital Myasthenic Syndromes |
|
Congenital Myasthenic Syndromes, Postsynaptic
|
|
|
| Congenital Myasthenic Syndrome |
|
Congenital Myasthenia
|
Congenital Myasthenic Syndromes
|
|
Cms
|
Myasthenic Syndromes, Congenital
|
|
Myasthenic Syndromes Congenital
|
Myasthenic Syndrome, Congenital
|
|
Congenital Myasthenic Syndrome Ib
|
Congenital And Developmental Myasthenia
|
|
Developmental Myasthenia
|
|
|
| Myasthenia Gravis |
|
MG
|
Acquired Myasthenia
|
|
Autoimmune Myasthenia Gravis
|
Erb-Goldflam Disease
|
|
Mg - [Myasthenia Gravis]
|
Myasthenia Gravis Nos
|
|
Myasthenia
|
|
|
| Neuromuscular Junction Disease |
|
Neuromuscular Junction Diseases
|
|
|
| Focal Segmental Glomerulosclerosis |
|
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome
|
Focal Glomerulosclerosis
|
|
Fsgs
|
Segmental Glomerulosclerosis
|
|
Glomerulosclerosis, Focal Segmental
|
Fgs
|
|
Focal Glomerular Sclerosis
|
Familial Idiopathic Nephrotic Syndrome
|
|
Focal Sclerosis With Hyalinosis
|
Glomerulosclerosis, Focal
|
|
Glomerulosclerosis Focal
|
Glomerulosclerosis, Segmental, Focal
|
|
Focal Segmental Glomerulosclerosis, Not Otherwise Specified
|
|
|
| Cenani-Lenz Syndactyly Syndrome |
|
Syndactyly Type 7
|
Cenani Syndactylism
|
|
Cenani-Lenz Syndactyly
|
CLSS
|
|
Syndactyly Cenani Lenz Type
|
Cenani-Lenz Syndrome
|
|
Syndactyly, Type Vii
|
Cenani-Lenz Type Syndactyly
|
|
Cenani Syndactyly
|
Syndactyly Type Vii
|
|
|
| Sclerosteosis 2 |
|
SOST2
|
Sclerosteosis, Type 2
|
|
|
| Pierson Syndrome |
|
Microcoria-Congenital Nephrotic Syndrome
|
Microcoria-Congenital Nephrosis Syndrome
|
|
PIERS
|
Microcoria - Congenital Nephrosis
|
|
Microcoria - Congenital Nephrotic Syndrome
|
PIERSS
|
|
|
| Muscular Dystrophy |
|
Muscular Dystrophies
|
Congenital Md
|
|
Congenital Muscular Dystrophy
|
Cmd
|
|
Mdc
|
Dystrophy, Muscular
|
|
Gower'S Muscular Dystrophy
|
Progressive Musclular Dystrophy
|
|
Pseudohypertrophic Atrophy
|
Pseudohypertrophic Muscle Paralysis
|
|
Pseudohypertrophic Muscular Atrophy
|
Pseudohypertrophic Muscular Dystrophy
|
|
Pseudohypertrophic Paralysis
|
Pseudomuscular Hypertrophy
|
|
|
| Neonatal Myasthenia Gravis |
|
Myasthenia Gravis, Neonatal
|
|
|
| Diffuse Mesangial Sclerosis |
|
Familial Mesangial Sclerosis
|
Mesangial Sclerosis, Diffuse
|
|
Dms
|
Diffuse Isolated Mesangial Sclerosis
|
|
Isolated Diffuse Mesangial Sclerosis
|
Nephrotic Syndrome, Early Onset With Diffuse Mesangial Sclerosis
|
|
|
| Muscular Dystrophy, Congenital Merosin-Deficient, 1a |
|
MDC1A
|
Lama2-Related Muscular Dystrophy
|
|
Atrophie Blanche
|
Muscular Dystrophy, Congenital Merosin-Deficient
|
|
Congenital Merosin-Deficient Muscular Dystrophy 1a
|
Merosin-Negative Congenital Muscular Dystrophy
|
|
Muscular Dystrophy White Matter Spongiosis
|
Merosin Deficient Congenital Muscular Dystrophy
|
|
Muscular Dystrophy Congenital, Merosin Negative
|
Muscular Dystrophy, Congenital, Merosin Deficient Or Partially Deficient
|
|
Cmd1a
|
Congenital Muscular Dystrophy Due To Laminin Alpha2 Deficiency
|
|
Congenital Muscular Dystrophy Type 1a
|
Laminin Alpha-2 Deficiency
|
|
Merosin-Deficient Congenital Muscular Dystrophy
|
Muscular Dystrophy, Congenital, Merosin-Deficient
|
|
Lama2 Md
|
Laminin Alpha 2 Deficiency
|
|
Laminin Alpha-2 Deficient Muscular Dystrophy
|
Merosin-Deficient Muscular Dystrophy
|
|
Muscular Dystrophy Due To Lama2 Deficiency
|
Merosin-Deficient Congenital Muscular Dystrophy 1a
|
|
Cardiomyopathy, Familial Idiopathic
|
|
|
| Nephrotic Syndrome, Type 5, With Or Without Ocular Abnormalities |
|
NPHS5
|
Nephrotic Syndrome Type 5
|
|
Nephrotic Syndrome Type 5, With Or Without Ocular Abnormalities
|
Nephrotic Syndrome 5 With Or Without Ocular Abnormalities
|
|
Nephrotic Syndrome, Type 5, With/Without Ocular Abnormalities
|
|
|
| Partial Optic Atrophy |
|
|
| Myasthenic Syndrome, Congenital, 5 |
|
Endplate Acetylcholinesterase Deficiency
|
Congenital Myasthenic Syndrome 5
|
|
CMS5
|
Ead
|
|
Engel Congenital Myasthenic Syndrome
|
Myasthenic Syndrome, Congenital, Engel Type
|
|
Cms Ic
|
Congenital Myasthenic Syndrome Type Ic
|
|
Congenital Myasthenic Syndrome Type Ic, Formerly
|
Cms1c, Formerly
|
|
Cms Ic, Formerly
|
Congenital Myasthenic Syndrome Engel Type
|
|
End Plate Acetylcholinesterase Deficiency
|
Synaptic Congenital Myasthenic Syndromes
|
|
Cms1c
|
Cmse
|
|
Congenital Myasthenic Syndrome Type 1c
|
End-Plate Acetylcholinesterase Deficiency
|
|
Myasthenic Syndrome, Congenital, Type 5
|
|
|
| Walker-Warburg Syndrome |
|
Hard Syndrome
|
Walker-Warburg Congenital Muscular Dystrophy
|
|
Cerebroocular Dysplasia-Muscular Dystrophy Syndrome
|
Cod-Md Syndrome
|
|
Chemke Syndrome
|
Hydrocephalus, Agyria And Retinal Dysplasia
|
|
Cerebroocular Dysgenesis
|
Cerebroocular Dysplasia Muscular Dystrophy Syndrome
|
|
Hard +/- E Syndrome
|
Pagon Syndrome
|
|
Warburg Syndrome
|
Hydrocephalus, Agyria, And Retinal Dysplasia
|
|
Mddga
|
Muscular Dystrophy-Dystroglycanopathy , Type A
|
|
Muscular Dystrophy-Dystroglycanopathy [With Brain And Eye Anomalies], Type A
|
Hydrocephalus-Agyria-Retinal Dysplasia Syndrome
|
|
Wws
|
Dystrophy, Muscular, Dystroglycanopathy, Type A
|
|
|
| Muscular Dystrophy-Dystroglycanopathy , Type B, 1 |
|
MDDGB1
|
Muscular Dystrophy-Dystroglycanopathy , Type B1
|
|
Muscular Dystrophy, Congenital, Pomt1-Related
|
Muscular Dystrophy-Dystroglycanopathy Type B1
|
|
Cmd Due To Dystroglycanopathy
|
Muscular Dystrophy-Dystroglycanopathy Congenital With Impaired Intellectual Development B1
|
|
Muscular Dystrophy Congenital Pomt1-Related
|
Muscular Dystrophy-Dystroglycanopathy
|
|
Dystrophy, Muscular, Dystroglycanopathy , Type B1
|
|
|
| Congenital Muscular Dystrophy-Dystroglycanopathy Type A |
|
Congenital Muscular Alpha-Dystroglycanopathy With Brain And Eye Anomalies
|
Mddga
|
|
Klissencephaly Type 2 With Muscular And Ocular Involvement
|
Lissencephaly Type 2 With Muscular And Ocular Involvement
|
|
|
| Muscular Dystrophy-Dystroglycanopathy , Type A, 4 |
|
Fukuyama Congenital Muscular Dystrophy
|
Fcmd
|
|
MDDGA4
|
Fukuyama Type Congenital Muscular Dystrophy
|
|
Walker-Warburg Syndrome Or Muscle-Eye-Brain Disease, Fktn-Related
|
Cerebromuscular Dystrophy, Fukuyama Type
|
|
Fukuyama Cmd
|
Fukuyama Muscular Dystrophy
|
|
Fukuyama Syndrome
|
Muscular Dystrophy, Congenital Progressive, With Mental Retardation
|
|
Muscular Dystrophy, Congenital, Fukuyama Type
|
Muscular Dystrophy, Congenital, With Central Nervous System Involvement
|
|
Polymicrogyria With Muscular Dystrophy
|
Congenital Muscular Dystrophy, Fukuyama Type
|
|
Fktn-Related Congenital Muscular Dystrophy
|
Muscular Dystrophy-Dystroglycanopathy Congenital With Brain And Eye Anomalies A4
|
|
Cerebromuscular Dystrophy Fukuyama Type
|
Congenital Muscular Dystrophy Fukuyama Type
|
|
Micropolygyria With Muscular Dystrophy
|
Muscle-Eye-Brain Disease Fktn-Related
|
|
Walker-Warburg Syndrome Fktn-Related
|
|
|
| Asperger Syndrome |
|
Asperger Disorder
|
Asperger Syndrome, Susceptibility To
|
|
|
| Autoimmune Disease Of Peripheral Nervous System |
|
|
| Thymus Gland Disease |
|
|
| Thymus Cancer |
|
Thymic Neoplasm
|
Thymic Tumor
|
|
Thymus Neoplasm
|
Thymus Neoplasms
|
|
Malignant Neoplasm Of Thymus
|
Neoplasm Of Thymus
|
|
Thymic Neoplasms
|
Thymoma, Familial
|
|
Thymic Carcinoma
|
Thymoma, Type C
|
|
Cancer Of Thymus
|
Malignant Tumour Of Thymus
|
|
Primary Malignant Neoplasm Of Thymus
|
Thymic Glandular Cancer
|
|
Thymus Gland Cancer
|
|
|
| Porencephaly |
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
| Autosomal Recessive Alport Syndrome |
|
Alport Syndrome, Recessive Type
|
Alport Syndrome, Autosomal Recessive
|
|
Alport Syndrome Autosomal Recessive
|
Alport Syndrome Recessive Type
|
|
Nephropathy And Deafness
|
|
|
| Alport Syndrome |
|
Hereditary Nephritis
|
Alport Syndrome, X-Linked
|
|
Hemorrhagic Hereditary Nephritis
|
Congenital Hereditary Hematuria
|
|
Hemorrhagic Familial Nephritis
|
Familial Nephritis
|
|
Thin Basement Membrane Disease
|
Thin Basement Membrane Nephropathy
|
|
Hematuria-Nephropathy-Deafness Syndrome
|
Hematuric Hereditary Nephritis
|
|
Hereditary Familial Congenital Hemorrhagic Nephritis
|
Hereditary Hematuria Syndrome
|
|
Hereditary Interstitial Pyelonephritis
|
Alport Deafness-Nephropathy
|
|
Alport Hearing Loss-Nephropathy
|
Alports Syndrome
|
|
Nephritis, Hereditary
|
|
|
| Autosomal Recessive Limb-Girdle Muscular Dystrophy |
|
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive
|
|
|
| Limb-Girdle Muscular Dystrophy |
|
Lgmd
|
Limb Girdle Muscular Dystrophy
|
|
Muscular Dystrophies, Limb-Girdle
|
Erb'S Muscular Dystrophy
|
|
Leyden-Mbius Muscular Dystrophy
|
Limb-Girdle Syndrome
|
|
Myopathic Limb-Girdle Syndrome
|
Limb Girdle
|
|
Muscular Dystrophy Limb-Girdle
|
Dystrophy, Muscular, Limb-Girdle
|
|
Lgmd - [Limb-Girdle Muscular Dystrophy]
|
Limb Girdle Muscle Dystrophy
|
|
Limb-Girdle Myopathy
|
|
|
| Ptosis |
|
Blepharoptosis
|
Drooping Eyelid
|
|
Droopy Eyelid
|
Ptosis Of Eyelid
|
|
Paralysis Of Levator Palpebrae Superioris
|
|
|
| Autosomal Recessive Intellectual Developmental Disorder |
|
Mental Retardation, Autosomal Recessive
|
Autosomal Recessive Mental Retardation
|
|
Autosomal Recessive Non-Syndromic Mental Retardation
|
Autosomal Recessive Non-Syndromic Intellectual Disability
|
|
|
| Alzheimer Disease, Familial, 1 |
|
Alzheimer Disease
|
Alzheimer'S Disease
|
|
Presenile And Senile Dementia
|
AD1
|
|
Alzheimer Disease, Susceptibility To
|
Alzheimer Disease, Late-Onset, Susceptibility To
|
|
Alzheimer Disease 1, Familial
|
AD
|
|
Familial Alzheimer Disease
|
Alzheimer Disease, Late-Onset
|
|
Alzheimers Dementia
|
Alzheimer Dementia
|
|
Alzheimer Sclerosis
|
Alzheimer Syndrome
|
|
Alzheimer-Type Dementia
|
Dat
|
|
Primary Senile Degenerative Dementia
|
Sdat
|
|
Alzheimer Disease 1
|
Autosomal Dominant Alzheimer Disease
|
|
Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy
|
Late Onset Alzheimer Disease
|
|
Alzheimers Disease
|
Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
|
|
Late-Onset Alzheimers Disease
|
Alzheimer'S Disease Pathway Kegg
|
|
Dementia Due To Alzheimer'S Disease
|
Alzheimer Disease Type 1
|
|
Alzheimers
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| Myopathy |
|
Muscular Diseases
|
Myopathies
|
|
|
| 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
|
|
|
