| Diseases |
Alias |
|
| Atransferrinemia |
|
Familial Hypotransferrinemia
|
Congenital Atransferrinemia
|
|
Hypotransferrinemia, Familial
|
Congenital Hypotransferrinemia
|
|
ATRAF
|
|
|
| Iron Overload In Africa |
|
African Iron Overload
|
Bantu Siderosis
|
|
African Hemochromatosis
|
Hereditary Iron Overload And African Americans
|
|
African Nutritional Hemochromatosis
|
African Siderosis
|
|
|
| Nutritional Deficiency Disease |
|
Malnutrition
|
Nutritional Disorder
|
|
Nutritional Deficiency
|
Nutrition
|
|
Deficiency Diseases
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
|
Nutrition Disorders
|
|
|
| Iron Metabolism Disease |
|
Iron Deficiency
|
Iron Disorder
|
|
Iron Metabolism Disorders
|
Disorder Of Iron Metabolism
|
|
Iron
|
Fe Deficiency
|
|
Iron Storage Disease
|
Iron Storage Disorder
|
|
|
| Iron Deficiency Anemia |
|
Iron-Deficiency Anemia
|
Fe Deficiency Anaemia
|
|
Ida - [Iron Deficiency Anemia]
|
Fe - [Iron] Deficiency Anemia Nos
|
|
|
| Siderosis |
|
Pulmonary Siderosis
|
Deposition Of Iron
|
|
Arc-Welders' Disease
|
Arc-Welders' Lung
|
|
Arc-Welders' Nodulation
|
Arc-Welders' Pneumoconiosis
|
|
Iron Oxide Lung
|
Iron Pneumoconiosis
|
|
Pneumoconiosis Siderotico
|
Siderotic Lung Disease
|
|
Steel Grinders' Disease
|
Welders' Lung
|
|
Welders' Siderosis
|
Lung Fibrosis With Siderosis
|
|
|
| Protein-Energy Malnutrition |
|
PEM
|
Protein Energy Malnutrition
|
|
|
| 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
|
|
|
| Microcytic Anemia |
|
Iron-Refractory Iron Deficiency Anemia
|
|
|
| Hfe Hemochromatosis |
|
Hemochromatosis Type 1
|
Hfe-Associated Hemochromatosis
|
|
Hfe-Hh
|
|
|
| Rare Hereditary Hemochromatosis |
|
Iron Overload
|
Iron Overload Disease
|
|
Idiopathic Haemosiderosis
|
Hemosiderosis
|
|
|
| Beta-Thalassemia |
|
Beta Thalassemia
|
Cooley'S Anemia
|
|
Mediterranean Anemia
|
Beta Thalassemia Intermedia
|
|
Erythroblastic Anemia
|
Thalassemia, Hispanic Gamma-Delta-Beta
|
|
Thalassemia Major
|
Thalassemia Minor
|
|
Beta-Plus-Thalassemia
|
Thalassemia, Beta
|
|
Beta Thalassemia Major
|
Beta Thalassemia Minor
|
|
Thalassemias, Beta-
|
Microcytemia, Beta Type
|
|
Thalassemia, Beta Type
|
B-THAL
|
|
Mediterranean Anaemia
|
Beta Thalassaemia Syndrome
|
|
Mediterranean Disease
|
Beta Thalassaemia Disease
|
|
|
| Haemophilus Influenzae |
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Liver Cirrhosis |
|
Cirrhosis
|
Cirrhosis Of Liver
|
|
CIRRH
|
Cryptogenic Cirrhosis
|
|
Cirrhosis, Cryptogenic
|
Cirrhosis Nos
|
|
|
| Congenital Disorder Of Glycosylation, Type Ia |
|
CDG1A
|
Cdg Ia
|
|
Phosphomannomutase 2 Deficiency
|
Jaeken Syndrome
|
|
Pmm2-Congenital Disorder Of Glycosylation
|
Congenital Disorder Of Glycosylation Type Ia
|
|
Cdgia
|
Congenital Disorder Of Glycosylation Ia
|
|
Congenital Disorder Of Glycosylation 1a
|
Carbohydrate-Deficient Glycoprotein Syndrome Type Ia
|
|
Cdgs1a
|
Pmm2-Cdg
|
|
Cdg-Ia
|
Congenital Disorder Of Glycosylation Type 1a
|
|
Carbohydrate-Deficient Glycoprotein Syndrome, Type Ia, Formerly
|
Pmm Deficiency
|
|
Cdg Syndrome Type Ia
|
Carbohydrate Deficient Glycoprotein Syndrome Type Ia
|
|
Cdg Syndrome Type 1a
|
Jaeken'S Syndrome
|
|
Pmm2 Deficiency
|
Glycosylation, Congenital Disorder Of, Type Ia
|
|
|
| Dysentery |
|
|
| Intracranial Hypotension |
|
|
| Alcohol Use Disorder |
|
Alcohol Abuse
|
Alcoholism
|
|
Ethanol Abuse
|
Alcohol Addiction
|
|
Alcohol Dependence
|
Alcoholic Intoxication, Chronic
|
|
Alcohol-Related Disorders
|
|
|
| Thalassemia |
|
Sickle-Cell Thalassemia With Crisis
|
Sickle-Cell Thalassemia Without Crisis
|
|
Thalassemia Hb-S Disease With Crisis
|
Thalassemia Hb-S Disease Without Crisis
|
|
Thalassemias
|
Hereditary Leptocytosis
|
|
Haemoglobin Thalassaemia Disorder
|
Thalassaemia Syndrome
|
|
Thalassaemia Nos
|
Thalassemia Variants
|
|
|
| Porphyria Cutanea Tarda |
|
Hepatoerythropoietic Porphyria
|
HEP
|
|
Uroporphyrinogen Decarboxylase Deficiency
|
Pct
|
|
Pct, Type Ii
|
Porphyria, Hepatocutaneous Type
|
|
Urod Deficiency
|
Porphyria, Hepatoerythropoietic
|
|
Porphyria Cutanea Tarda, Susceptibility To
|
Familial Porphyria Cutanea Tarda
|
|
Porphyria Cutanea Tarda, Type Ii
|
Pct, 'Familial' Type
|
|
Porphyria, Hepatic
|
FPCT
|
|
Pct Type Ii
|
Porphyria Cutanea Tarda Type Ii
|
|
Porphyria Hepatocutaneous Type
|
Heterozygous Uroporphyrinogen Decarboxylase Deficiency
|
|
Urod - [Uroporphyrinogen Decarboxylase] Deficiency
|
Pct - [Porphyria Cutanea Tarda]
|
|
|
| Hemosiderosis |
|
Haemosiderosis
|
Iron Overload
|
|
|
| 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
|
|
|
| Hyperferritinemia With Or Without Cataract |
|
Hyperferritinemia-Cataract Syndrome
|
Hhcs
|
|
Hereditary Hyperferritinemia With Congenital Cataracts
|
Hyperferritinemia, Hereditary, With Congenital Cataracts
|
|
Bonneau-Beaumont Syndrome
|
HRFTC
|
|
Hereditary Hyperferritinemia-Cataract Syndrome
|
Cataract-Hyperferritinemia Syndrome
|
|
Hyperferritinemia Cataract Syndrome
|
Hereditary Hyperferritinemia Cataract Syndrome
|
|
|
| Chronic Kidney Disease |
|
Chronic Renal Disease
|
Chronic Kidney Failure
|
|
Ckd
|
Chronic Renal Failure
|
|
Kidney Failure, Chronic
|
Chronic Renal Failure Syndrome
|
|
Crf
|
Renal Failure - Chronic
|
|
Renal Failure Chronic
|
Chronic Kidney Diseases
|
|
Chronic Kidney Disease Stage 5
|
Ckd - [Chronic Kidney Disease]
|
|
Crf - [Chronic Renal Failure]
|
Chronic Kidney Impairment
|
|
Chronic Renal Impairment
|
Chronic Kidney Shutdown
|
|
Chronic Hypoxic Kidney Failure
|
Chronic Kidney Collapse
|
|
Chronic Renal Insufficiency
|
Chronic Kidney Toxaemia
|
|
Chronic Kidney Hypofunction
|
Chronic Renal Suppression
|
|
Chronic Renal Failure, Stage 5
|
Ckd - [Chronic Kidney Disease] Stage 5
|
|
End Stage Kidney Failure
|
End Stage Renal Failure
|
|
End Stage Kidney Disease
|
End Stage Renal Disease
|
|
End Stage Chronic Renal Failure
|
Esrf - [End Stage Renal Failure]
|
|
Esrd - [End Stage Renal Diseases]
|
Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
|
|
|
| Liver Disease |
|
Liver Failure
|
Liver Diseases
|
|
Abnormality Of The Liver
|
Liver Dysfunction
|
|
Disorder Of Liver
|
Hepatic Disorder
|
|
Hepatic Disease
|
Disease Of Bilirubin Metabolism
|
|
Disorder Of Bilirubin Metabolism
|
Liver Decompensation
|
|
Liver Function Failure
|
Hepatic Failure Nos
|
|
Liver Failure Nos
|
End Stage Liver Disease
|
|
Decompensated Liver Failure
|
Decompensation Of Liver Function
|
|
Hepatic Decompensation
|
Hepatic Insufficiency
|
|
Liver Cell Necrosis With Hepatic Failure
|
Liver Insufficiency
|
|
Decompensated Liver Disease
|
End Stage Liver Failure
|
|
Liver Necrosis With Hepatic Failure
|
|
|
| Cholera |
|
Vibrio Cholerae Infection
|
Cholera - Vibrio Cholerae
|
|
Cholera Due To Vibrio Cholerae
|
Vibrio Cholerae
|
|
Cholera Syndrome
|
Asiatic Cholera
|
|
Epidemic Cholera
|
|
|
| Hypochromic Microcytic Anemia |
|
Anemia, Hypochromic Microcytic
|
Microcytic Hypochromic Anemia
|
|
|
| Kidney Disease |
|
Renal Failure
|
Kidney Failure
|
|
Kidney Diseases
|
Nephropathy
|
|
Abnormality Of The Kidney
|
Impaired Renal Function Disease
|
|
Renal Anomaly
|
Kidney Dysfunction
|
|
Renal Disease
|
Nephropathies
|
|
Renal Failure Adverse Event
|
Abnormal Renal Function
|
|
|
| Substance Abuse |
|
Substance-Related Disorders
|
Substance Abuse Problem
|
|
|
| Congenital Disorder Of Glycosylation, Type In |
|
Congenital Disorder Of Glycosylation
|
CDG1N
|
|
Congenital Disorders Of Glycosylation
|
Cdg In
|
|
Cdgin
|
Congenital Disorder Of Glycosylation 1n
|
|
Carbohydrate-Deficient Glycoprotein Syndrome
|
Cdg
|
|
Rft1-Cdg
|
Cdg-In
|
|
Congenital Disorder Of Glycosylation Type In
|
Carbohydrate Deficient Glycoprotein Syndrome
|
|
Cdg Syndrome
|
Congenital Disorder Of Glycosylation In
|
|
Carbohydrate-Deficient Glycoprotein Syndromes
|
Cdg Syndrome Type In
|
|
Carbohydrate Deficient Glycoprotein Syndrome Type In
|
Congenital Disorder Of Glycosylation Type 1n
|
|
Man5glcnac2-Pp-Dol Flippase Deficiency
|
Glycosylation, Congenital Disorder Of
|
|
Glycosylation, Congenital Disorder Of, Type In
|
|
|
| Analbuminemia |
|
ANALBA
|
Congenital Analbuminemia
|
|
Hypoalbuminemia
|
|
|
| Adult Respiratory Distress Syndrome |
|
Acute Respiratory Distress Syndrome
|
Ards
|
|
Non-Cardiogenic Pulmonary Edema
|
Acute Lung Injury
|
|
Respiratory Distress Syndrome, Adult
|
Shock Lung
|
|
Acute Respiratory Distress
|
Respiratory Distress Syndrome
|
|
Adult Rds
|
Ali
|
|
Increased-Permeability Pulmonary Edema
|
Stiff Lung
|
|
Respiratory Distress Syndrome Adult
|
|
|
| Trypanosomiasis |
|
|
| Sleeping Sickness |
|
African Trypanosomiasis
|
African Sleeping Sickness
|
|
Trypanosomiasis, Human East-African
|
Trypanosomiasis, East African
|
|
Trypanosomiasis African
|
Trypanosomiasis, African
|
|
Human African Trypanosomiasis
|
|
|
| Congenital Hemolytic Anemia |
|
Anemia Hemolytic Congenital
|
Anemia, Hemolytic, Congenital
|
|
Congenital Hemolytic Anaemia
|
Hereditary Hemolytic Anaemia
|
|
Hereditary Hemolytic Anemia
|
|
|
| Interstitial Lung Disease |
|
Ild
|
Lung Diseases, Interstitial
|
|
Lung Diseases Interstitial
|
Interstitial Lung Diseases
|
|
|
| Hemolytic Anemia |
|
Anemia, Hemolytic
|
Anemia Hemolytic
|
|
Anaemia Due To Other Disorders Of Glutathione Metabolism
|
Chronic Non Spherocytic Anaemia
|
|
G6pd - [Glucose-6-Phosphate Dehydrogenase Deficiency] Anaemia
|
Anaemia Due To Glucose-6-Phosphate Dehydrogenase Deficiency
|
|
Glucose-6-Phosphate Dehydrogenase Deficiency With Anaemia
|
Glucose-6-Phosphate Dehydrogenase Deficiency Anaemia
|
|
Favism Anaemia
|
Haemolytic Anaemia Due Tog6pd Deficiency
|
|
Favism
|
Pentose Phosphate Pathway Disorder Anaemia
|
|
Anaemia Due To Pentose Phosphate Pathway Defect
|
|
|
| Hemoglobinopathy |
|
|
| Lipoid Nephrosis |
|
Minimal Change Disease
|
Minimal Change Glomerulonephritis
|
|
Nephrotic Syndrome With Lesion Of Minimal Change Glomerulonephritis
|
Nephrotic Syndrome With Lesion Of Minimal Change Nephrotic Syndrome
|
|
Idiopathic Minimal Change Nephrotic Syndrome
|
Mcns
|
|
Minimal Change Glomerulopathy
|
Minimal Change Nephrotic Syndrome
|
|
Nephrotic Syndrome Minimal Change
|
Nephrosis, Lipoid
|
|
Glomerulonephritis, Minimal Change
|
Nephrotic Syndrome, Minimal Change
|
|
|
| Nephrotic Syndrome |
|
Finnish Congenital Nephrotic Syndrome
|
Ns - [Nephrotic Syndrome]
|
|
Nephrosis Syndrome
|
Nephrosis Nos
|
|
Glomerular Lesion Nephrosis
|
|
|
| Histoplasmosis |
|
Darling Disease
|
Reticuloendotheliosis, X-Linked
|
|
Infection By Histoplasma Capsulatum
|
Histoplasma Infection
|
|
Reticuloendothelial Cytomycosis
|
Cytomycosis
|
|
Darling Histoplasmosis
|
African Histoplasmosis
|
|
Histoplasmosis Duboisii
|
|
|
| Proctitis |
|
Ulcerative Proctitis
|
Chronic Ulcerative Proctitis
|
|
Idiopathic Proctitis
|
Nonspecific Ulcerative Proctitis
|
|
Ulcerative Colitis Confined To Rectum
|
Ip - [Idiopathic Proctitis]
|
|
Chronic Ulcerative Proctitis Nos
|
|
|
| Androgen Insensitivity Syndrome |
|
Androgen Resistance Syndrome
|
AIS
|
|
Testicular Feminization Syndrome
|
Androgen Receptor Deficiency
|
|
Dhtr Deficiency
|
Dihydrotestosterone Receptor Deficiency
|
|
Ar Deficiency
|
Testicular Feminization
|
|
Tfm
|
Androgen Insensitivity
|
|
Androgen-Insensitivity Syndrome
|
Goldberg-Maxwell Syndrome
|
|
Complete Androgen Insensitivity Syndrome
|
Cais
|
|
Feminisation - Testicular
|
Goldberg - Maxwell Syndrome
|
|
Androgen Insensitivity Syndrome, Complete
|
Morris Syndrome
|
|
Ary
|
AR
|
|
Insensitivity Syndrome, Androgen
|
Androgen Insensitivity Nos
|
|
|
| Osebold-Remondini Syndrome |
|
Brachydactyly Type A6
|
Brachymesophalangy With Mesomelic Short Limbs And Carpal And Tarsal Osseous Abnormalities
|
|
Bda6
|
Brachydactyly, Type A6
|
|
|
| Scrapie |
|
|
| Marasmus |
|
Nutritional Marasmus
|
Nutritional Atrophy
|
|
|
| Cystinosis |
|
Cystine Storage Disease
|
Cystine Diathesis
|
|
Cystine Disease
|
Cystinoses
|
|
Protein Defect Of Cystin Transport
|
Cystin Transport, Protein Defect Of
|
|
Nephropathic Cystinosis
|
Protein Defect Of Cystine Transport
|
|
|
| Diabetes Mellitus |
|
|
| Vitreoretinopathy, Neovascular Inflammatory |
|
Proliferative Vitreoretinopathy
|
Adniv
|
|
Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy
|
VRNI
|
|
Pvr
|
Neovascular Inflammatory Vitreoretinopathy
|
|
Vitreoretinopathy, Neovascular Inflammatory, Autosomal Dominant
|
Retinitis Proliferans
|
|
Neovascular Inflammatory Vitreoretinopathy Autosomal Dominant
|
Vitreoretinopathy Proliferative
|
|
Vitreoretinopathy, Proliferative
|
Proliferative Vitreo-Retinopathy
|
|
|
| Type 2 Diabetes Mellitus |
|
Insulin Resistance
|
NIDDM
|
|
Type 2 Diabetes
|
Diabetes Mellitus, Non-Insulin-Dependent
|
|
T2D
|
Noninsulin-Dependent Diabetes Mellitus
|
|
Diabetes Mellitus, Type Ii
|
Maturity-Onset Diabetes
|
|
Insulin Resistance, Severe, Digenic
|
Diabetes Mellitus, Type 2
|
|
Diabetes Mellitus, Noninsulin-Dependent
|
Diabetes Mellitus, Noninsulin-Dependent, Association With
|
|
Diabetes Mellitus, Noninsulin-Dependent, Late Onset
|
Hypertension, Insulin Resistance-Related, Susceptibility To
|
|
Insulin Resistance, Susceptibility To
|
Non-Insulin-Dependent Diabetes Mellitus
|
|
Type Ii Diabetes Mellitus
|
Adult-Onset Diabetes Mellitus
|
|
Maturity-Onset Diabetes Mellitus
|
Diabetes Mellitus Type 2
|
|
Type Ii Diabetes
|
Type 2 Diabetes Mellitus, Susceptibility To
|
|
Diabetes, Type 2
|
Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To
|
|
Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 2, Susceptibility To
|
|
Diabetes Mellitus, Noninsulin-Dependent, 2
|
Diabetes Mellitus, Type Ii, Susceptibility To
|
|
Hypertension, Insulin Resistance-Related
|
Adult-Onset Diabetes
|
|
Aodm
|
Diabetes Mellitus, Adult-Onset
|
|
Diabetes Mellitus Type Ii
|
Diabetes Mellitus Type 2, Susceptibility To
|
|
Diabetes, Type Ii, Susceptibility To
|
Diabetes Type 2
|
|
Diabetes Mellitus
|
Adult Onset Diabetes
|
|
Maturity Onset Diabetes
|
Nonketotic Diabetes
|
|
Non-Insulin Dependent Diabetes Mellitus
|
T2dm - [Type 2 Diabetes Mellitus]
|
|
Niddm - [Non Insulin Dependent Diabetes Mellitus]
|
Dm2
|
|
Dm Type Ii
|
Diabetic Type 2
|
|
Insulin Requiring Type 2 Diabetes
|
Noninsulin Dependent Diabetes
|
|
Non-Insulin-Dependent Diabetes Mellitus Without Complications
|
Diabetes Due To Insulin Secretory Defect
|
|
Diabetes Mellitus Due To Insulin Secretory Defect
|
Non-Insulin-Dependent Diabetes Of The Young
|
|
Senile Diabetes
|
Nonketotic Hyperglycaemia
|
|
Stable Diabetes
|
|
|
| Cataract |
|
Cataracts
|
Cat - [Cataract]
|
|
Cataract Form
|
Lens Opacity
|
|
Lens Opacities
|
|
|
| Myelodysplastic Syndrome |
|
Myelodysplastic Syndromes
|
Myelodysplasia
|
|
MDS
|
Myelodysplastic Syndrome Included
|
|
Myelodysplastic Syndrome, Susceptibility To, Included
|
Myelodysplastic Syndrome, Somatic
|
|
Myelodysplastic Syndrome, Susceptibility To
|
|
|
| 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
|
|
|
