Diseases |
Alias |
|
Glaucoma, Primary Open Angle |
Glaucoma 1, Open Angle, E
|
Primary Open Angle Glaucoma
|
POAG
|
Adult-Onset Primary Open Angle Glaucoma
|
Chronic Simple Glaucoma
|
GLC1E
|
Primary Open Angle Glaucoma 1e
|
Glaucoma, Open Angle, Primary
|
|
|
Amyotrophic Lateral Sclerosis 12 With Or Without Frontotemporal Dementia |
|
|
Glaucoma, Normal Tension |
Low Tension Glaucoma
|
Glaucoma, Normal Tension, Susceptibility To
|
Normal Tension Glaucoma
|
Ntg
|
Glaucoma, Normal Pressure
|
NPG
|
Glaucoma, Normal Pressure, Susceptibility To
|
Poag/Npg - [Normal Pressure Primary Open-Angle Glaucoma]
|
|
|
Amyotrophic Lateral Sclerosis Type 12 |
Amyotrophic Lateral Sclerosis 12
|
Als12
|
Sclerosis, Lateral, Amyotrophic, Type Type 12
|
|
|
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
|
|
|
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
|
|
|
Open-Angle Glaucoma |
Glaucoma Simplex
|
Pigmentary Glaucoma
|
Wide-Angle Glaucoma
|
Glaucoma, Open-Angle
|
Open Angle Glaucoma
|
Glaucoma Open-Angle
|
Chronic Simple Glaucoma
|
Coag - [Chronic Open-Angle Glaucoma]
|
Csg - [Chronic Simple Glaucoma]
|
Poag - [Primary Open-Angle Glaucoma]
|
Oag - [Open-Angle Glaucoma]
|
Chronic Glaucoma
|
Chronic Open Angle Glaucoma
|
Simple Glaucoma
|
Chronic Noncongestive Glaucoma
|
Ltg - [Low Tension Glaucoma]
|
Noncongestive Glaucoma
|
Nonobstructive Glaucoma
|
Normal Pressure Glaucoma
|
Primary Low Tension Glaucoma
|
Low-Tension Glaucoma
|
Residual Stage Low Tension Glaucoma
|
Open Cleft Glaucoma
|
|
|
Frontotemporal Dementia |
Pallidopontonigral Degeneration
|
Frontotemporal Lobar Degeneration
|
Semantic Dementia
|
FTD
|
Frontotemporal Lobe Dementia
|
Multiple System Tauopathy With Presenile Dementia
|
Dementia, Frontotemporal
|
Frontotemporal Dementia With Parkinsonism
|
Mstd
|
Frontotemporal Lobar Degeneration With Tau Inclusions
|
Ftld With Tau Inclusions
|
Dementia, Frontotemporal, With Parkinsonism
|
Fldem
|
Ftdp17
|
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex
|
Ddpac
|
Wilhelmsen-Lynch Disease
|
Wld
|
Ppnd
|
Dementia, Frontotemporal, With Or Without Parkinsonism
|
Semantic Primary Progressive Aphasia
|
Semantic Variant Ppa
|
Wilhemsen-Lynch Disease
|
Frontotemporal Dementia-Amyotrophic Lateral Sclerosis
|
Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17
|
Ftd-Als
|
Ftld
|
Pick Complex
|
Pick Disease Of The Brain
|
Frontotemporal Dementia With Parkinsonism-17
|
Grn-Related Frontotemporal Dementia
|
Frontotemporal Dementia With Motor Neuron Disease
|
Dementia In Fronto-Temporal Lobar Degeneration
|
Ftd - [Frontotemporal Dementia]
|
Temple Dementia
|
Frontal Lobe Dementia
|
|
|
Intraocular Pressure Quantitative Trait Locus |
Glaucoma
|
IOPQTL
|
Glaucoma, Susceptibility To
|
Postinfectious Glaucoma
|
Glaucoma With Ocular Inflammation
|
Glaucoma Secondary To Eye Inflammation
|
Traumatic Glaucoma
|
Glaucoma With Concussion Of Globe
|
Glaucoma Due To Ocular Trauma
|
Glaucoma Associated With Ocular Trauma
|
Glaucoma Secondary To Drugs
|
|
|
Glaucoma 1, Open Angle, A |
GLC1A
|
Joag1
|
Glaucoma, Primary Open Angle, Juvenile-Onset, 1
|
Glaucoma 1a, Primary Open Angle
|
Primary Open Angle Glaucoma Juvenile Onset 1
|
Glaucoma Hereditary, Juvenile
|
Juvenile-Onset Primary Open Angle Glaucoma 1
|
Primary Open Angle Glaucoma 1a
|
Glaucoma, Open Angle, Type 1a
|
|
|
Glaucoma 3, Primary Congenital, A |
Buphthalmos
|
Glaucoma, Congenital
|
Congenital Glaucoma
|
Glaucoma 3a, Primary Open Angle, Congenital, Juvenile, Or Adult Onset
|
GLC3A
|
Glc3
|
Buphthalmia
|
Primary Congenital Glaucoma
|
Glaucoma, Primary Open Angle, Juvenile-Onset
|
Simple Buphthalmos
|
Buphthalmus
|
Glaucoma, Primary Open Angle, Adult-Onset
|
Primary Congenital Glaucoma 3a
|
Primary Infantile Glaucoma Type 3a
|
Glaucoma 3a, Primary Congenital
|
Glaucoma, Congenital, Primary, Type 3a
|
Hydrophthalmos
|
Cystic Eyeball
|
|
|
Ocular Hypertension |
Hypertension, Ocular
|
Intraocular Pressure Increase
|
Oh - [Ocular Hypertension]
|
Oht - [Ocular Hypertension]
|
|
|
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
|
|
|
Lateral Sclerosis |
Primary Lateral Sclerosis
|
Adult-Onset Primary Lateral Sclerosis
|
Adult-Onset Pls
|
Motor Neuron Disease
|
Pls
|
Pls - [Primary Lateral Sclerosis]
|
Lateral Spinal Sclerosis
|
Lateral Complete Paralysis
|
Lateral Incomplete Paralysis
|
Lateral Paralysis
|
|
|
Dementia |
Dementias
|
Presenile Dementia
|
Alzheimer Type Dementia
|
Alzheimer Sclerosis
|
Alzheimer Disease Dementia
|
Alzheimer Dementia
|
Primary Degenerative Alzheimer Type Dementia
|
End Stage Alzheimer'S Dementia
|
Alzheimer'S Type Atypical Dementia
|
Alzheimer Type Presenile Dementia
|
Early Onset Alzheimer Dementia
|
Dementia In Alzheimer Disease Type 2
|
Dementia In Alzheimer Disease With Early Onset
|
Early Onset Alzheimer Type Dementia, Uncomplicated
|
Primary Degenerative Alzheimer Type Dementia, Early Onset
|
Primary Degenerative Alzheimer Type Dementia, Presenile Onset, Uncomplicated
|
Alzheimer Disease Dementia With Early Onset
|
Presenile Sclerosis
|
Presenile Brain Sclerosis
|
Presenile Alzheimer Brain Sclerosis
|
Late Onset Alzheimer Dementia
|
Dementia In Alzheimer Disease Type 1
|
Dementia In Alzheimer Disease With Late Onset
|
Primary Degenerative Alzheimer Type Dementia, Late Onset
|
Sdat - [Senile Dementia, Alzheimer Type]
|
Alzheimer Disease Dementia With Late Onset
|
Late Onset Alzheimer Brain Sclerosis
|
Senile Alzheimer Brain Disease
|
Senile Alzheimer Brain Sclerosis
|
Senile Primary Degenerative Alzheimer Type Dementia
|
Senile Dementia Of The Alzheimer Type
|
Arteriosclerotic Dementia
|
Strategic-Infarct Dementia
|
Post Stroke Dementia
|
Vascular Cognitive Impairment
|
Vascular Dementia
|
Dementia Of The Lewy Body Type
|
Dementia With Lewy Bodies
|
Sdlt - [Senile Dementia Of The Lewy Body Type]
|
Senile Dementia Of The Lewy Body Type
|
Alcohol-Related Dementia
|
Alcoholic Dementia Nos
|
Alcohol-Induced Dementia
|
Alcoholic Brain Syndrome
|
Chronic Alcoholic Brain Syndrome
|
Alcohol Dementia
|
Late Onset Alcoholic Psychosis
|
Residual And Late-Onset Alcohol-Induced Psychotic Disorder
|
Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder
|
Late-Onset Psychoactive Substance-Induced Psychotic Disorder
|
Inhalant Dementia
|
Volatile Solvents Dementia
|
Dementia In Paralysis Agitans
|
Pdd - [Parkinson Disease Dementia]
|
Dementia Syndrome Of Parkinson Disease
|
Dementia In Parkinson Disease
|
Parkinson Related Dementia
|
Dementia In Huntington Chorea
|
Hiv - [Human Immunodeficiency Virus] Dementia
|
Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex
|
Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex
|
Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex
|
Aids Related Dementia
|
Dementia Due To Niacin Deficiency
|
|
|
Aphasia |
|
|
Neuropathy |
Peripheral Neuropathy
|
Peripheral Neuropathies
|
|
|
Paget'S Disease Of Bone |
Osteitis Deformans
|
Paget Disease Of Bone
|
Osseous Paget'S Disease
|
Paget Disease Of Bone, Familial
|
Bone Paget Disease
|
Familial Paget'S Disease Of Bone
|
Paget'S Bone Disease
|
Familial Paget Disease Of Bone
|
Paget Disease, Bone
|
Pdb
|
Pagets Bone Disease
|
|
|
Juvenile Glaucoma |
Glaucoma Of Childhood
|
Hydrophthalmos
|
|
|
Spinocerebellar Ataxia 2 |
Spinocerebellar Ataxia Type 2
|
SCA2
|
Amyotrophic Lateral Sclerosis 13
|
Spinocerebellar Degeneration With Slow Eye Movements
|
SDSEM
|
Spinocerebellar Atrophy Ii
|
Olivopontocerebellar Atrophy Ii
|
Opca2
|
Cerebellar Degeneration With Slow Eye Movements
|
Wadia-Swami Syndrome
|
Amyotrophic Lateral Sclerosis Type 13
|
ALS13
|
Olivopontocerebellar Atrophy Holguin Type
|
Spinocerebellar Ataxia Cuban Type
|
Olivopontocerebellar Atrophy, Holguin Type
|
Spinocerebellar Ataxia, Cuban Type
|
Amyotrophic Lateral Sclerosis, Susceptibility To, 13
|
Olivopontocerebellar Atrophy 2
|
Sca 2
|
Spinocerebellar Ataxia With Slow Eye Movements
|
Spinocerebellar Atrophy 2
|
Wadia Swami Syndrome
|
Opca Ii
|
Spinocerebellar Ataxia-2
|
Ataxia, Spinocerebellar, Type 2
|
|
|
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
|
|
|
Primary Congenital Glaucoma |
|
|
Amyotrophic Lateral Sclerosis Type 15 |
Amyotrophic Lateral Sclerosis 15, With Or Without Frontotemporal Dementia
|
Als15
|
Amyotrophic Lateral Sclerosis 15
|
|
|
Eye Disease |
Eye Diseases
|
Abnormality Of The Eye
|
Toxoplasma Oculopathy
|
|
|
Amyotrophic Lateral Sclerosis Type 14 |
Als14
|
Amyotrophic Lateral Sclerosis 14
|
Amyotrophic Lateral Sclerosis, With Or Without Frontotemporal Dementia
|
Amyotrophic Lateral Sclerosis 14 With Or Without Frontotemporal Dementia
|
|
|
Acute Closed-Angle Glaucoma |
Acute Angle-Closure Glaucoma
|
|
|
Multisystem Proteinopathy |
|
|
Phacogenic Glaucoma |
|
|
Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia |
Amyotrophic Lateral Sclerosis Type 10
|
ALS10
|
Amyotrophic Lateral Sclerosis 10, With Or Without Ftd
|
Frontotemporal Lobar Degeneration, Tardbp-Related
|
Amyotrophic Lateral Sclerosis 10
|
Amyotrophic Lateral Sclerosis 10, With Or Without Frontotemporal Dementia
|
Tardbp-Related Frontotemporal Lobar Degeneration With Tdp43 Inclusions
|
Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia And With Tdp43 Inclusions
|
Sclerosis, Lateral, Amyotrophic, Type Type 10
|
|
|
Steroid-Induced Glaucoma |
Corticosteroid-Induced Glaucoma
|
|
|
Amyotrophic Lateral Sclerosis 11 |
Amyotrophic Lateral Sclerosis Type 11
|
ALS11
|
Sclerosis, Lateral, Amyotrophic, Type Type 11
|
|
|
Primary Angle-Closure Glaucoma |
Primary Angle Closure Glaucoma
|
Angle Closure Glaucoma
|
Acg - [Angle Closure Glaucoma]
|
Angle-Closure Glaucoma
|
Closed Angle Glaucoma
|
Acute Glaucoma
|
Prodromal Angle Closure Glaucoma
|
|
|
Amyotrophic Lateral Sclerosis 16, Juvenile |
Amyotrophic Lateral Sclerosis Type 16
|
ALS16
|
Amyotrophic Lateral Sclerosis 16
|
Sclerosis, Lateral, Amyotrophic, Type 16, Juvenile
|
|
|
Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia |
Ibmpfd
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia
|
Pagetoid Amyotrophic Lateral Sclerosis
|
Pagetoid Neuroskeletal Syndrome
|
Inclusion Body Myopathy With Paget Disease Of Bone And/Or Frontotemporal Dementia
|
Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone And/Or Frontotemporal Dementia
|
Multisystem Proteinopathy
|
Limb-Girdle Muscular Dystrophy With Paget Disease Of Bone
|
Inclusion Body Myopathy With Paget'S Disease Of Bone And Frontotemporal Dementia
|
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dement
|
Lower Motor Neuron Degeneration With Paget-Like Bone Disease
|
Muscular Dystrophy, Limb-Girdle, With Paget Disease Of Bone
|
Myopathy, Inclusion Body, With Early-Onset Paget Disease And Frontotemporal Dementia
|
|
|
Progressive Muscular Atrophy |
Progressive Spinal Muscular Atrophy
|
Pure Progressive Muscular Atrophy
|
Pma
|
Hereditary Spinal Muscle Atrophy
|
Pma - [Progressive Muscular Atrophy]
|
Progressive Muscle Atrophy
|
Progressive Spinal Muscle Atrophy
|
Duchenne-Aran Atrophy
|
Duchenne-Aran Muscle Atrophy
|
Hereditary Sma - [Spinal Muscle Atrophy]
|
|
|
Amyotrophic Lateral Sclerosis 8 |
Amyotrophic Lateral Sclerosis Type 8
|
ALS8
|
Sclerosis, Lateral, Amyotrophic, Type Type 8
|
|
|
Mammary Paget'S Disease |
Paget'S Disease
|
Mammary Paget Disease
|
Paget'S Disease Of The Breast
|
Paget Disease Of The Breast
|
Paget'S Disease Of The Nipple
|
Paget'S Disease, Mammary
|
Paget Cell Neoplasm
|
Paget Disease Of The Nipple
|
Pagets Disease Mammary
|
Osteitis Deformans
|
|
|
Amyotrophic Lateral Sclerosis Type 6 |
Amyotrophic Lateral Sclerosis 6, Autosomal Recessive
|
Als6
|
Amyotrophic Lateral Sclerosis 6, With Or Without Frontotemporal Dementia
|
Autosomal Recessive Amyotrophic Lateral Sclerosis 6
|
Sclerosis, Lateral, Amyotrophic, Type Type 6
|
Amyotrophic Lateral Sclerosis 6
|
|
|
Keratitis, Hereditary |
Keratitis
|
Autosomal Dominant Keratitis
|
Hereditary Keratitis
|
Dominantly Inherited Keratitis
|
Keratitis Hereditary
|
KERH
|
|
|
Retinal Degeneration |
|
|
Cranial Nerve Disease |
Cranial Nerve Disorder
|
Disorder Of Cranial Nerve
|
Cranial Nerve Diseases
|
|
|
Giant Axonal Neuropathy 2 |
|
|
Hemochromatosis, Type 1 |
Hemochromatosis
|
Hemochromatosis Type 1
|
Hereditary Hemochromatosis
|
Hh
|
HFE1
|
Hfe Hemochromatosis, Modifier Of
|
Symptomatic Form Of Classic Hemochromatosis
|
Symptomatic Form Of Hemochromatosis Type 1
|
Symptomatic Form Of Hfe-Related Hereditary Hemochromatosis
|
Haemochromatosis
|
Iron Storage Disorder
|
Bronze Diabetes
|
Hereditary Haemochromatosis
|
Hlah
|
Hfe
|
Hemochromatosis, Hereditary
|
Diabetes Bronze
|
Classic Hemochromatosis
|
Hfe-Associated Hereditary Hemochromatosis
|
Hemochromatosis Classic
|
Bronzed Cirrhosis
|
Familial Hemochromatosis
|
Genetic Hemochromatosis
|
Hc
|
Pigmentary Cirrhosis
|
Primary Hemochromatosis
|
Troisier-Hanot-Chauffard Syndrome
|
Von Recklenhausen-Applebaum Disease
|
Hemochromatosis 1
|
Primary Hereditary Hemochromatosis
|
Bronze Cirrhosis
|
|
|
Pick Disease Of Brain |
Pick Disease
|
Pick'S Disease
|
Pick Disease Of The Brain
|
Lobar Atrophy Of Brain
|
Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions
|
Behavioral Variant Of Frontotemporal Dementia
|
Dementia In Pick'S Disease
|
Lobar Atrophy Of The Brain
|
Bvftd
|
Bv-Ftd
|
PIDB
|
Picks Disease
|
|
|
Breast Adenocarcinoma |
Mammary Adenocarcinoma
|
Adenocarcinoma Of Breast
|
|
|
Leber Hereditary Optic Neuropathy, Modifier Of |
Leber Optic Atrophy
|
Leber Hereditary Optic Neuropathy
|
LHON
|
Leber'S Hereditary Optic Neuropathy
|
Leber Optic Atrophy, Susceptibility To
|
Leber'S Optic Atrophy
|
LOAM
|
Loas
|
Leber'S Disease
|
Leber'S Optic Neuropathy
|
Optic Atrophy, Hereditary, Leber
|
Lhon, Modifier Of
|
Optic Atrophy, Leber Type
|
Hereditary Optic Neuroretinopathy
|
Leber Hereditary Optic Atrophy
|
Loa
|
Optic Atrophy Leber Type
|
Leber Hereditary Optic Neuropathy, Modifier
|
Leber Hereditary Optic Neuropathy Susceptibility
|
Modifier Of Leber Hereditary Optic Neuropathy
|
Lebers Hereditary Optic Neuropathy
|
Leber Congenital Amaurosis
|
|
|
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
|
|
|
Peripheral Nervous System Disease |
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
Nervous System Disease |
Abnormality Of The Nervous System
|
Nervous System Diseases
|
Nervous System Disorder
|
|
|
Retinitis Pigmentosa |
RP
|
Rod-Cone Dystrophy
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
Tapetoretinal Degeneration
|
Rcd
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|