| Diseases |
Alias |
|
| Epilepsy, Nocturnal Frontal Lobe, 1 |
|
ENFL1
|
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 1
|
|
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
|
Nocturnal Frontal Lobe Epilepsy 1
|
|
Adnfle
|
Epilepsy, Frontal Lobe, Nocturnal, Type 1
|
|
Epilepsy, Nocturnal Frontal Lobe, Type 1
|
|
|
| Autosomal Dominant Nocturnal Frontal Lobe Epilepsy |
|
Adnfle
|
Autosomal Dominant Sleep-Related Hypermotor Epilepsy
|
|
Enfl
|
Benign Familial Infantile Seizures 6
|
|
Benign Familial Infantile Seizures, 6
|
Nocturnal Frontal Lobe Epilepsy-4
|
|
Enfl1
|
Epilepsy, Nocturnal Frontal Lobe, 1
|
|
Epilepsy, Nocturnal Frontal Lobe, Type 1
|
|
|
| Tobacco Addiction |
|
Nicotine Dependence
|
Tobacco Addiction, Susceptibility To
|
|
Nicotine Addiction
|
Tobacco Use Disorder
|
|
Smoking Habit
|
Nicotine Dependence, Protection Against
|
|
Nicotine Addiction, Protection From
|
Cigarette Habituation
|
|
Cigarette Habituation, Susceptibility To
|
Smoking Habit, Susceptibility To
|
|
Nicotine Dependence, Susceptibility To
|
Nicotine Addiction, Susceptibility To
|
|
Addiction, Tobacco, Susceptibility To
|
Compulsive Tobacco User Syndrome
|
|
Tobacco Dependence
|
Tobacco Dependence Syndrome
|
|
Cigarette Addiction
|
Cigarette Dependence
|
|
Smoking Addiction
|
Smokers Syndrome
|
|
|
| Epilepsy |
|
Epilepsy Syndrome
|
Epileptic Syndrome
|
|
Epilepsies
|
Symptomatic Epilepsies
|
|
Post Traumatic Epilepsy
|
Traumatic Epilepsy
|
|
Traumatic Epileptic
|
Epilepsy Due To Hippocampal Sclerosis
|
|
Epilepsy With Ammon'S Horn Sclerosis
|
Epilepsy Due To Cortical Dysplasia
|
|
Epilepsy Due To Neuronal Migration Disorders
|
|
|
| Benign Familial Neonatal Epilepsy |
|
Familial Neonatal Seizures
|
Bfns
|
|
Benign Familial Neonatal Convulsions
|
Benign Familial Neonatal Seizures
|
|
Epilepsy Benign Neonatal Familial
|
Familial Benign Neonatal Convulsions
|
|
Benign Neonatal Familial Convulsions
|
Familial Benign Neonatal Epilepsy
|
|
Epilepsy, Benign Neonatal, 2
|
Benign Familial Convulsion
|
|
|
| Focal Epilepsy |
|
Partial Epilepsy
|
Epilepsies, Partial
|
|
Localisation-Related Epilepsy
|
|
|
| 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
|
|
|
| Epilepsy, Idiopathic Generalized |
|
Idiopathic Generalized Epilepsy
|
Generalised Epilepsy
|
|
Epilepsy, Generalized
|
EIG
|
|
Ige
|
Epilepsy, Idiopathic Generalized, Susceptibility To, 1
|
|
Epilepsy, Idiopathic Generalized 1
|
Epilepsy, Idiopathic Generalized, Susceptibility To
|
|
Epilepsy, Idiopathic, Generalized
|
Epilepsy, Idiopathic, Generalized, Susceptibility To, Type 1
|
|
|
| Epilepsy, Myoclonic Juvenile |
|
Juvenile Myoclonic Epilepsy
|
Janz Syndrome
|
|
Jme
|
Myoclonic Epilepsy, Juvenile, Susceptibility To, 1
|
|
EJM
|
Myoclonic Epilepsy, Juvenile
|
|
Petit Mal, Impulsive
|
Myoclonic Epilepsy, Juvenile 1
|
|
Myoclonic Epilepsy, Juvenile, 1
|
Adolescent Myoclonic Epilepsy
|
|
Juvenile Myoclonus Epilepsy
|
Juvenile Myoclonic Epilepsy 1
|
|
EJM1
|
Petit Mal Impulsive
|
|
Susceptibility To Juvenile Myoclonic Epilepsy 1
|
Myoclonic Epilepsy Juvenile
|
|
Epilepsy, Myoclonic, Juvenile
|
Myoclonic Epilepsy Of Janz
|
|
Jme - [Juvenile Myoclonic Epilepsy]
|
|
|
| Childhood Absence Epilepsy |
|
Pyknolepsy
|
Petit Mal Epilepsy
|
|
Absence Seizures
|
Absence Seizure
|
|
Petit Mal Seizure
|
Absence Epilepsy, Childhood
|
|
Pykno-Epilepsy
|
Epilepsy, Absence
|
|
Absence Epilepsy
|
Pycnolepsy
|
|
|
| Reflex Epilepsy |
|
Epilepsy, Reflex
|
Epilepsy, Sensory-Induced
|
|
Epilepsy Reflex
|
|
|
| Attention Deficit-Hyperactivity Disorder |
|
Attention Deficit Hyperactivity Disorder
|
ADHD
|
|
Attention Deficit Disorder
|
Attention Deficit-Hyperactivity Disorder, Susceptibility To
|
|
Attention Deficit Disorder With Hyperactivity
|
Hyperkinetic Disorder
|
|
Hyperactivity Of Childhood
|
Attention-Deficit/Hyperactivity Disorder
|
|
Add
|
Addh
|
|
Attention Deficit
|
Attention Deficit Disorder Of Childhood With Hyperactivity
|
|
Attention Deficit Disorder With Hyperactivity Syndrome
|
Hyperkinetic Syndrome
|
|
Attention-Deficit Hyperactivity Disorder
|
Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type
|
|
Disturbance Of Activity And Attention
|
Disorder Of Activity And Attention
|
|
Adhd - [Attention Deficit Hyperactivity Disorder]
|
Hyperkinetic Disorders
|
|
Disorder Of Activity And Attention With Hyperkinesia
|
Attention Deficit Syndrome With Hyperactivity
|
|
|
| Epilepsy, Nocturnal Frontal Lobe, 2 |
|
Epilepsy, Nocturnal Frontal Lobe, Type 2
|
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 2
|
|
ENFL2
|
Nocturnal Frontal Lobe Epilepsy 2
|
|
|
| Early Myoclonic Encephalopathy |
|
Myoclonic Epilepsy
|
Myoclonic Seizure
|
|
Epilepsies, Myoclonic
|
Epileptic Seizures - Myoclonic
|
|
Epileptic Seizures, Myoclonic
|
Myoclonia Epileptica
|
|
Myoclonic Seizure Disorder
|
Early Myoclonic Encephalopathy With Suppression-Bursts
|
|
|
| Benign Neonatal Seizures |
|
Benign Neonatal Epilepsy
|
Benign Familial Neonatal Seizures
|
|
Benign Neonatal Convulsions
|
Benign Familial Neonatal Convulsions
|
|
Benign Familial Neonatal Epilepsy
|
Bfne
|
|
Bfns
|
Seizures, Benign Neonatal
|
|
Neonatal Convulsions Benign
|
Epilepsy, Benign Neonatal
|
|
Epilepsy, Benign Neonatal, 2
|
Benign Familial Convulsion
|
|
Familial Benign Neonatal Epilepsy
|
|
|
| Exfoliation Syndrome |
|
Pseudoexfoliation Glaucoma
|
Pseudoexfoliation Syndrome
|
|
Exfoliation Syndrome, Susceptibility To
|
XFS
|
|
Exfoliation Glaucoma
|
Xfg
|
|
Pseudoexfoliation Of The Lens
|
Pexg
|
|
Pexs
|
Exfoliative Syndrome
|
|
Glaucoma Capsulare
|
Pex
|
|
Pseudo-Exfoliation Syndrome
|
|
|
| Developmental And Epileptic Encephalopathy 7 |
|
Epileptic Encephalopathy, Early Infantile, 7
|
DEE7
|
|
Eiee7
|
Kcnq2-Related Epileptic Encephalopathy
|
|
Kcnq2-Related Neonatal Epileptic Encephalopathy
|
Developmental And Epileptic Encephalopathy, 7
|
|
Early Infantile Epileptic Encephalopathy 7
|
Kcnq2-Nee
|
|
Ohtahara Syndrome
|
Encephalopathy, Epileptic, Early Infantile, Type 7
|
|
Early Infantile Epileptic Encephalopathy With Suppression Bursts
|
|
|
| Arthrogryposis, Distal, Type 2a |
|
Freeman-Sheldon Syndrome
|
Craniocarpotarsal Dystrophy
|
|
Craniocarpotarsal Dysplasia
|
DA2A
|
|
Whistling Face-Windmill Vane Hand Syndrome
|
Fss
|
|
Distal Arthrogryposis Type 2a
|
Whistling Face Syndrome
|
|
Freeman-Burian Syndrome
|
Arthrogryposis Distal Type 2a
|
|
Distal Arthrogryposis, Type 2a
|
Fbs
|
|
Arthrogryposis, Distal, 2a
|
|
|
| Early Onset Absence Epilepsy |
|
|
| Benign Familial Infantile Epilepsy |
|
Benign Familial Infantile Seizures
|
Bfie
|
|
Benign Familial Infantile Convulsion
|
Bfic
|
|
Bfis
|
Benign Familial Infantile Convulsions
|
|
Familial Benign Neonatal Epilepsy
|
Watanabe-Vigevano Syndrome
|
|
|
| Hypotrichosis-Lymphedema-Telangiectasia Syndrome |
|
HLTS
|
Hypotrichosis Lymphedema Telangiectasia Syndrome
|
|
Hypotrichosis-Lymphedema-Telangiectasia-Membranoproliferative Glomerulonephritis Syndrome
|
Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome
|
|
|
| Juvenile Absence Epilepsy |
|
Epilepsy Juvenile Absence
|
Jae
|
|
Childhood Absence Epilepsy
|
Absence Epilepsy
|
|
|
| Adolescence-Adult Electroclinical Syndrome |
|
|
| Developmental And Epileptic Encephalopathy 14 |
|
Malignant Migrating Partial Seizures Of Infancy
|
Eiee14
|
|
Epilepsy Of Infancy With Migrating Focal Seizures
|
Mmpsi
|
|
DEE14
|
Epileptic Encephalopathy, Early Infantile, 14
|
|
Early Infantile Epileptic Encephalopathy 14
|
Malignant Migrating Partial Epilepsy Of Infancy
|
|
Migrating Partial Epilepsy Of Infancy
|
Migrating Partial Seizures Of Infancy
|
|
Mmpei
|
Mpei
|
|
Mpsi
|
Malignant Migrating Focal Seizures Of Infancy
|
|
Migrating Partial Seizures In Infancy
|
Developmental And Epileptic Encephalopathy, 14
|
|
Encephalopathy, Epileptic, Early Infantile, Type 14
|
|
|
| Unverricht-Lundborg Syndrome |
|
Unverricht-Lundborg Disease
|
Epm1
|
|
Myoclonic Epilepsy Of Unverricht And Lundborg
|
Myoclonus Progressive Epilepsy Of Unverricht And Lundborg
|
|
Unverricht - Lundborg Disease
|
Unverricht'S Disease
|
|
Epilepsy, Progressive Myoclonic Type 1
|
Epilepsy, Progressive Myoclonus 1
|
|
Progressive Myoclonus Epilepsy Baltic Myoclonic Epilepsy
|
Baltic Myoclonic Epilepsy
|
|
Baltic Myoclonus
|
Baltic Myoclonus Epilepsy
|
|
Lundborg-Unverricht Syndrome
|
Mediterranean Myoclonic Epilepsy
|
|
Pme
|
Progressive Myoclonic Epilepsy
|
|
Progressive Myoclonus Epilepsy 1
|
Uld
|
|
Myoclonic Epilepsies, Progressive
|
|
|
| Generalized Epilepsy With Febrile Seizures Plus |
|
Gefs+
|
Genetic Epilepsy With Febrile Seizures Plus
|
|
Generalized Epilepsy With Febrile Seizures-Plus
|
Genetic Epilepsy With Febrile Seizures-Plus
|
|
Epilepsy, Generalized, With Febrile Seizures Plus
|
|
|
| Substance Dependence |
|
|
| Episodic Kinesigenic Dyskinesia 1 |
|
Paroxysmal Kinesigenic Choreoathetosis
|
Paroxysmal Kinesigenic Dyskinesia
|
|
Dystonia 10
|
Familial Paroxysmal Kinesigenic Dyskinesia
|
|
Episodic Kinesigenic Dyskinesia
|
EKD1
|
|
Pkc
|
Pkd
|
|
Dyt10
|
Familial Pkd
|
|
Paroxysmal Kinesigenic Choreathetosis
|
Familial Paroxysmal Dystonia
|
|
Dystonia, Familial Paroxysmal
|
Dyt-Prrt2
|
|
Dystonia, Type 10
|
|
|
| Familial Febrile Seizures |
|
Familial Febrile Convulsions
|
Feb
|
|
Febrile Seizures, Familial
|
|
|
| Epilepsy, Familial Temporal Lobe, 1 |
|
ETL1
|
Adpeaf
|
|
Adlte
|
Epilepsy, Partial, With Auditory Features
|
|
Autosomal Dominant Partial Epilepsy With Auditory Features
|
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant
|
|
Familial Temporal Lobe Epilepsy 1
|
Partial Epilepsy With Auditory Features
|
|
Autosomal Dominant Lateral Temporal Lobe Epilepsy
|
Lateral Temporal Lobe Epilepsy Autosomal Dominant
|
|
Epilepsy, Temporal Lobe, Familial, Type 1
|
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Childhood Electroclinical Syndrome |
|
|
| Neonatal Period Electroclinical Syndrome |
|
|
| Benign Epilepsy With Centrotemporal Spikes |
|
Rolandic Epilepsy
|
Benign Rolandic Epilepsy
|
|
Epilepsy, Rolandic
|
Bcects
|
|
Benign Childhood Epilepsy With Centrotemporal Spike
|
Sylvan Seizures
|
|
Becrs
|
Bects
|
|
Bre
|
Benign Epilepsy Of Childhood With Centrotemporal Spikes
|
|
Benign Familial Epilepsy Of Childhood With Rolandic Spikes
|
Centrotemporal Epilepsy
|
|
|
| Dravet Syndrome |
|
Severe Myoclonic Epilepsy Of Infancy
|
Severe Myoclonic Epilepsy In Infancy
|
|
Smei
|
Epileptic Encephalopathy, Early Infantile, 6
|
|
DRVT
|
Developmental And Epileptic Encephalopathy 6a
|
|
Dee6a
|
Eiee6
|
|
Developmental And Epileptic Encephalopathy, 6
|
Dee6
|
|
Developmental And Epileptic Encephalopathy 6
|
Early Infantile Epileptic Encephalopathy 6
|
|
Myoclonic Epilepsy, Severe, Of Infancy
|
Sme
|
|
Severe Myoclonus Epilepsy Of Infancy
|
Borderline Smei
|
|
Smeb
|
Smeb-M
|
|
Smeb-O
|
Smeb-Sw
|
|
Smei-Borderland
|
Smei-Borderland More Than One Feature
|
|
Smei-Borderland-Myoclonic Seizures
|
Smei-Borderland-Spike Wave
|
|
Intractable Childhood Epilepsy With Generalized Tonic-Clonic Seizures
|
ICEGTC
|
|
Infantile Severe Myoclonic Epilepsy
|
Epilepsy, Intractable Childhood, With Generalized Tonic-Clonic Seizures
|
|
|
| Developmental And Epileptic Encephalopathy |
|
Encephalopathy, Developmental And Epileptic
|
|
|
| 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
|
|
|
