| Diseases |
Alias |
|
| Personality Disorder |
|
Personality Disorders
|
Character Disorder
|
|
Personality
|
Specific Personality Disorders
|
|
Enduring Personality Change After Psychiatric Illness
|
|
|
| Major Depressive Disorder |
|
Seasonal Affective Disorder
|
Unipolar Depression
|
|
Depression
|
MDD
|
|
Depressive Disorder
|
Unipolar Depression, Susceptibility To
|
|
Major Depressive Disorder 1
|
Major Depressive Disorder, Response To Citalopram Therapy In
|
|
Major Depressive Disorder 2
|
Winter Depression
|
|
Single Major Depressive Episode
|
Sad
|
|
Clinical Depression
|
Major Depression
|
|
Depressive Syndrome
|
Major Depressive Disorder And Accelerated Response To Antidepressant Drug Treatment
|
|
Seasonal Affective Disorder, Susceptibility To
|
Recurrent Major Depression
|
|
Affective Disorder, Seasonal
|
Depression In A Seasonal Pattern
|
|
Depression
|
Seasonal
|
|
Major Depressive Disorder With A Seasonal Pattern
|
Seasonal Depression
|
|
Seasonal Mood Disorder
|
Mental Depression
|
|
Recurrent Major Depressive Episodes
|
|
|
| Bipolar Disorder |
|
Bipolar Depression
|
Manic Disorder
|
|
Depression, Bipolar
|
Bipolar Disorder Manic Phase
|
|
Depressive-Manic Psych.
|
Manic Bipolar Affective Disorder
|
|
Manic Bipolar I Disorder
|
Manic Depression
|
|
Manic Depressive Disorder
|
Mixed Bipolar Disorder
|
|
Bipolar Affective Disorder
|
Bipolar Affective Psychosis
|
|
Bipolar Spectrum Disorder
|
Manic Depressive Illness
|
|
Depression Bipolar
|
Bipolar Disorder, Mixed
|
|
Major Affective Disorder
|
Major Affective Disorder 1
|
|
Major Affective Disorder 2
|
|
|
| Anxiety |
|
Anxiety Disorder
|
Anxiety Disorders
|
|
Anxiety State
|
Anxieties
|
|
Anxiety Neurosis
|
|
|
| Generalized Anxiety Disorder |
|
|
| Hyperphenylalaninemia |
|
|
| Mast Cell Neoplasm |
|
Mastocytoma
|
Mast Cell Proliferative Disease
|
|
Mast Cell Tumor
|
Benign Mastocytoma
|
|
|
| Borderline Personality Disorder |
|
|
| Irritable Bowel Syndrome |
|
Irritable Colon
|
Psychogenic Ibs
|
|
Ibs - [Irritable Bowel Syndrome]
|
Spastic Bowel Syndrome
|
|
|
| Panic Disorder |
|
Panic Anxiety Syndrome
|
Panic
|
|
Panic Disorder 1
|
Episodic Paroxysmal Anxiety Disorder
|
|
|
| Obsessive-Compulsive Disorder |
|
OCD
|
Obsessive-Compulsive Disorder, Susceptibility To
|
|
Anancastic Neurosis
|
Obsessive Compulsive Disorder
|
|
Anankastic Neurosis
|
Obsessive-Compulsive Neurosis
|
|
Obsessive Compulsive Behavior
|
|
|
| Mood Disorder |
|
Mood Disorders
|
Episodic Mood Disorder
|
|
|
| Conduct Disorder |
|
|
| Brunner Syndrome |
|
Monoamine Oxidase A Deficiency
|
Antisocial Behavior
|
|
BRNRS
|
Deficiency Of Monoamine Oxidase A
|
|
X-Linked Monoamine Oxidase Deficiency
|
Susceptibility To Antisocial Behavior
|
|
Antisocial Behavior, Susceptibility To
|
Anti-Social Behavior
|
|
|
| Alcohol Dependence |
|
Alcoholism
|
Alcohol Dependence, Susceptibility To
|
|
Alcohol Dependence, Protection Against
|
Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against
|
|
Alcoholism, Susceptibility To
|
Alcoholic Intoxication, Chronic
|
|
Pharyngeal Neoplasms
|
Chronic Alcoholism
|
|
Dipsomania
|
Alcohol Addiction
|
|
Ethanol Dependence
|
Chronic Ethanolism
|
|
Chronic Alcoholic Disease Nos
|
Alcoholic Disease Nos
|
|
Alcoholic
|
|
|
| Autoimmune Polyendocrine Syndrome, Type I, With Or Without Reversible Metaphyseal Dysplasia |
|
APS1
|
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy
|
|
Apeced
|
Pga I
|
|
Hypoadrenocorticism With Hypoparathyroidism And Superficial Moniliasis
|
Autoimmune Polyendocrinopathy Syndrome , Type I, With Or Without Reversible Metaphyseal Dysplasia
|
|
Polyglandular Autoimmune Syndrome, Type 1
|
Autoimmune Polyglandular Syndrome Type 1
|
|
Autoimmune Polyendocrine Syndrome Type 1
|
Autoimmune Polyendocrinopathy Syndrome Type 1
|
|
Whitaker Syndrome
|
Aps Type 1
|
|
Polyglandular Type I Autoimmune Syndrome
|
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Syndrome
|
|
Aps I
|
Autoimmune Polyglandular Syndrome, Type I
|
|
Polyglandular Autoimmune Syndrome, Type I
|
Aps 1
|
|
Autoimmune Polyglandular Syndrome Type I
|
Pga 1
|
|
Pga-I
|
Polyglandular Autoimmune Syndrome Type 1
|
|
Type I Polyglandular Autoimmune Syndrome
|
Aire Deficiency
|
|
Autoimmune Polyendocrinopathy With Candidiasis And Ectodermal Dystrophy
|
Autoimmune Polyglandular Syndrome, Type 1
|
|
Autoimmune Polyendocrinopathy Type 1
|
Apeced Syndrome
|
|
Autoimmune Hypoparathyroidism-Chronic Candidiasis-Addison Disease Syndrome
|
Ham Syndrome
|
|
Hypoparathyroidism-Addison Disease-Mucocutaneous Candidiasis Syndrome
|
Medac Syndrome
|
|
Multiple Endocrine Deficiency-Addison Disease-Candidiasis Syndrome
|
Autoimmune Polyendocrine Syndrome 1, With Or Without Reversible Metaphyseal Dysplasia
|
|
Aps-1
|
Autoimmune Polyendocrine Syndrome Type I
|
|
Autoimmune Polyendocrinopathy Syndrome Type I
|
Autosomal Dominant Autoimmune Polyendocrinopathy Syndrome Type I
|
|
Polyglandular Autoimmune Syndrome Type I
|
Polyglandular Deficiency Syndrome Persian-Jewish Type
|
|
Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant
|
Polyendocrinopathy Autoimmune, Type 1, With/Without Reversible Metaphyseal Dysplasia
|
|
|
| Sudden Infant Death Syndrome |
|
SIDS
|
Sudden Infant Death Syndrome, Susceptibility To
|
|
Cot Death
|
Crib Death
|
|
Sudden Death Of Nonspecific Cause In Infancy
|
Sudden Infant Death
|
|
Death, Sudden, Syndrome, Infant
|
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Phenylketonuria |
|
Phenylalanine Hydroxylase Deficiency
|
PKU
|
|
Pah Deficiency
|
Folling Disease
|
|
Maternal Phenylketonuria
|
Phenylketonurias
|
|
Oligophrenia Phenylpyruvica
|
Hyperphenylalaninemia, Non-Pku Mild
|
|
Folling'S Disease
|
Phenylalaninemia
|
|
Mild Phenylketonuria
|
Mild Pku
|
|
Variant Pku
|
Variant Phenylketonuria
|
|
Mpku
|
Deficiency Disease, Phenylalanine Hydroxylase
|
|
Phenylketonuria, Maternal
|
Phenylalanine Hydroxylase Deficiency Disease
|
|
Hyperphenylalaninemic Embryopathy
|
Maternal Pku
|
|
Maternal Hyperphenylalaninemia
|
Phenylketonuric Embryopathy
|
|
Hyperphenylalaninemia
|
HPA
|
|
Non-Phenylketonuria Hyperphenylalaninemia
|
NON-PKU HPA
|
|
Phenylketonuria Maternal
|
Classical Phenylketonuria
|
|
Hyperphenylalaninaemia
|
Pku - [Phenylketonuria]
|
|
|
| Substance Dependence |
|
|
| Thyroid Dyshormonogenesis 1 |
|
TDH1
|
Hypothyroidism, Congenital, Due To Dyshormonogenesis, 1
|
|
Genetic Defect In Thyroid Hormonogenesis 1
|
Thyroid Hormonogenesis, Genetic Defect In, 1
|
|
Iodine Accumulation, Transport, Or Trapping Defect
|
Iodide Accumulation, Transport, Or Trapping Defect
|
|
Chdh1
|
Congenital Hypothyroidism Due To Dyshormonogenesis Type 1
|
|
Iodine Accumulation, Transport Or Trapping Defect
|
|
|
| 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
|
|
|
| Hypoadrenocorticism, Familial |
|
Addison Disease
|
Primary Adrenocortical Insufficiency
|
|
Addison'S Disease
|
Adrenal Gland Hypofunction
|
|
Adrenal Hypoplasia
|
Adrenal Aplasia
|
|
Addison Disease, Chronic Adrenal Insufficiency
|
Primary Hypoadrenalism
|
|
Hypoadrenocorticism Familial
|
Autoimmune Addison Disease
|
|
Autoimmune Adrenalitis
|
Classic Addison Disease
|
|
Primary Addison Disease
|
Addisons Disease
|
|
Addison Disease, Susceptibility To
|
Autoimmune Primary Adrenal Insufficiency
|
|
Addison'S Disease Due To Autoimmunity
|
|
|
| Anorexia Nervosa |
|
Anorexia Nervosa, Susceptibility To
|
ANON
|
|
Anorexia Nervosa, Susceptibility To, 1
|
An
|
|
Anorexia Nervosa 1
|
An - [Anorexia Nervosa]
|
|
|
| Wissler-Fanconi Syndrome |
|
Wissler'S Syndrome
|
Wissler'S Subsepsis Allergica
|
|
|
| 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
|
|
|
| Pulmonary Hypertension |
|
Primary Pulmonary Hypertension
|
Hypertension Pulmonary
|
|
Hypertension, Pulmonary
|
Hypertension, Pulmonary, Primary
|
|
Idiopathic Pulmonary Hypertension
|
Idiopathic Pulmonary Arterial Hypertension
|
|
Pulmonary Htn - [Hypertension]
|
|
|
| Psychotic Disorder |
|
Psychotic Disorders
|
Mental Or Behavioural Disorder
|
|
Psychotic
|
Mental Disorders
|
|
|
| Hypertryptophanemia |
|
HYPTRP
|
Hypertryptophanemia, Familial
|
|
Familial Hypertryptophanemia
|
|
|
| Narcolepsy |
|
Paroxysmal Sleep
|
Gelineau Syndrome
|
|
Narcoleptic Syndrome
|
Narcolepsy-Cataplexy Syndrome
|
|
Cataplexy And Narcolepsy
|
Narcolepsy, Without Cataplexy
|
|
Gelineau'S Syndrome
|
Narcolepsy With Or Without Cataplexy
|
|
Narcolepsy Nos
|
|
|
| Diarrhea |
|
Diarrhoea
|
Diarrhea Of Presumed Infectious Origin
|
|
|
| Dystonia, Dopa-Responsive, Due To Sepiapterin Reductase Deficiency |
|
Sepiapterin Reductase Deficiency
|
Spr Deficiency
|
|
Dopa-Responsive Dystonia Due To Sepiapterin Reductase Deficiency
|
Srd
|
|
Drd Due To Srd
|
Dopa-Responsive Hypersomnia
|
|
Dyt-Spr
|
Dyt/Park-Spr
|
|
Sr-Deficient Drd
|
Autosomal Recessive Sepiapterin Reductase-Deficient Drd
|
|
Spr
|
DRDSPRD
|
|
Motor And Cognitive Disorder Due To Sepiapterin Reductase Deficiency
|
Psychomotor Disorders
|
|
|
| Microscopic Colitis |
|
|
| Endogenous Depression |
|
Clinical Depression
|
Unipolar Depression
|
|
Depressive Disorder
|
|
|
| Lymphocytic Colitis |
|
|
| Scoliosis |
|
|
| Migraine With Or Without Aura 1 |
|
Migraine
|
Migraine With Or Without Aura, Susceptibility To, 1
|
|
Migraine Disorder
|
Migraine Variant
|
|
Migraines
|
Migraine Disorders
|
|
Mgr1
|
Mgau
|
|
Ma
|
Migraine With Or Without Aura
|
|
Classic Migraine
|
Common Migraine
|
|
Disorder, Migraine
|
Headache Migraine
|
|
Headache Migrainous
|
Migraine Headache
|
|
Migraine Syndrome
|
Headache Including Migraine
|
|
Migraine, Susceptibility To
|
|
|
| Hyperphenylalaninemia, Bh4-Deficient, A |
|
6-Pyruvoyl-Tetrahydropterin Synthase Deficiency
|
Pts Deficiency
|
|
HPABH4A
|
Hyperphenylalaninemia, Tetrahydrobiopterin-Deficient, Due To Pts Deficiency
|
|
Ptsd
|
Bh4-Deficient Hyperphenylalaninemia A
|
|
Hyperphenylalaninemia Due To 6-Pyruvoyltetrahydropterin Synthase Deficiency
|
Tetrahydobioperin-Deficient Hyperphenylalaninemia Due To Pts Deficiency
|
|
Hyperphenylalanemia, Bh4-Deficient, A
|
Hyperphenylalaninemia Due To 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency
|
|
6-Pyruvoyltetrahydropterin Synthase Deficiency
|
Hyperphenylalaninemia Tetrahydrobiopterin-Deficient Due To Pts Deficiency
|
|
Ptpsd
|
Hyperphenylalaninemia, Bh4-Deficient, Type A
|
|
|
| Ischemic Colitis |
|
Colitis, Ischemic
|
Irreversible Ischaemic Colitis
|
|
|
| Mental Depression |
|
Depression
|
Depressive Disorder
|
|
|
| Melancholia |
|
|
| Rett Syndrome |
|
Atypical Rett Syndrome
|
RTT
|
|
Rett Disorder
|
Rts
|
|
Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use
|
Rett Syndrome, Preserved Speech Variant
|
|
Rett Syndrome, Atypical
|
Rett'S Disorder
|
|
Rett Syndrome Variant
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome
|
|
Cerebroatrophic Hyperammonemia
|
Rett Like Syndrome
|
|
Rett'S Syndrome
|
Atypical Rtt
|
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use
|
Rett Syndrome Preserved Speech Variant
|
|
Rett Syndrome Zappella Variant
|
Rett Syndrome, Zappella Variant
|
|
|
| Dystonia 12 |
|
DYT12
|
Rdp
|
|
Generalized Dystonia
|
Dystonia-12
|
|
Rapid-Onset Dystonia-Parkinsonism
|
Familial Dystonia
|
|
Dystonia Musculorum Deformans
|
Dystonic Disorders
|
|
Idiopathic Familial Dystonia
|
Dystonia-Parkinsonism, Rapid-Onset
|
|
Fragments Of Torsion Dystonia
|
Dyt-Atp1a3
|
|
Rapid-Onset Dystonia Parkinsonism
|
Rodp
|
|
Dystonia, Type 12
|
Dystonia 3, Torsion, X-Linked
|
|
Idiopathic Non-Familial Dystonia
|
Symptomatic Torsion Dystonia
|
|
Dystonia Disorders
|
|
|
| Aromatic L-Amino Acid Decarboxylase Deficiency |
|
Aadc Deficiency
|
Dopa Decarboxylase Deficiency
|
|
Ddc Deficiency
|
Aromatic Amino Acid Decarboxylase Deficiency
|
|
Deficiency Of Aromatic-L-Amino-Acid Decarboxylase
|
AADCD
|
|
Aromatic-L-Amino-Acid Decarboxylase Deficiency
|
Aromatic L-Amino-Acid Decarboxylase Deficiency
|
|
|
| Type 1 Diabetes Mellitus 2 |
|
Diabetes Mellitus, Noninsulin-Dependent, 1
|
Diabetes Mellitus, Insulin-Dependent, 2
|
|
IDDM2
|
Insulin-Dependent Diabetes Mellitus 2
|
|
NIDDM1
|
Diabetes Mellitus, Noninsulin-Dependent 1
|
|
T1D2
|
Type 2 Diabetes Mellitus 1
|
|
T2D1
|
Noninsulin-Dependent Diabetes Mellitus 1
|
|
Diabetes Mellitus, Non-Insulin-Dependent, 1
|
Type 2 Diabetes Mellitus 1, Susceptibility To
|
|
Diabetes Mellitus, Insulin-Dependent, Type 2
|
Diabetes Mellitus, Non-Insulin-Dependent
|
|
|
| Dystonia |
|
Dystonic Disease
|
Dystonic Disorder
|
|
Dystonia Disorders
|
Neuroleptic Dyskinesia
|
|
|
| Parkinson Disease, Late-Onset |
|
Parkinson Disease
|
Parkinson'S Disease
|
|
PD
|
PARK
|
|
Parkinson Disease, Susceptibility To
|
Late Onset Parkinson'S Disease
|
|
Late Onset Parkinson Disease
|
Paralysis Agitans
|
|
Primary Parkinsonism
|
Idiopathic Parkinson Disease
|
|
Parkinson'S
|
Parkinson Disease, Late-Onset, Susceptibility To
|
|
Parkinson Disease, Age Of Onset, Modifier
|
Lewy Body Parkinson Disease
|
|
Idiopathic Parkinson'S Disease
|
Pd - [Parkinson Disease]
|
|
Parkinson Disease Nos
|
Parkinson, Nos
|
|
Primary Parkinson Disease
|
|
|
| Constipation |
|
|
| 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
|
|
|
