| 疾病名称 |
别名 |
|
| Immunodeficiency 46 |
|
Tfrc-Related Combined Immunodeficiency
|
IMD46
|
|
Cid Due To Tfrc Deficiency
|
Combined Immunodeficiency Due To Tfrc Deficiency
|
|
|
| Combined Immunodeficiency |
|
Combined T Cell And B Cell Immunodeficiency
|
Congenital Combined Immunodeficiency
|
|
Syndrome With Combined Immunodeficiency
|
Combined T And B Cell Immunodeficiency
|
|
Combined Immunity Deficiency
|
Combined Immunodeficiency Syndrome
|
|
Combined T-Cell And B-Cell Immunodeficiency
|
Lymphopenic Agammaglobulinaemia
|
|
|
| Combined T And B Cell Immunodeficiency |
|
|
| Iron Deficiency Anemia |
|
Iron-Deficiency Anemia
|
Fe Deficiency Anaemia
|
|
Ida - [Iron Deficiency Anemia]
|
Fe - [Iron] Deficiency Anemia Nos
|
|
|
| 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
|
|
|
| Iron Metabolism Disease |
|
Iron Deficiency
|
Iron Disorder
|
|
Iron Metabolism Disorders
|
Disorder Of Iron Metabolism
|
|
Iron
|
Fe Deficiency
|
|
Iron Storage Disease
|
Iron Storage Disorder
|
|
|
| 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
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| 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
|
|
|
| Anemia, Sideroblastic, 1 |
|
Xlsa
|
X-Linked Sideroblastic Anemia
|
|
Hypochromic Anemia
|
Anh1
|
|
Hereditary Iron-Loading Anemia
|
Anemia, Sideroblastic, X-Linked
|
|
Anemia, Hereditary Sideroblastic
|
Erythroid 5-Aminolevulinate Synthase Deficiency
|
|
Hereditary Sideroblastic Anemia
|
SIDBA1
|
|
Anemia, Hypochromic
|
Sideroblastic Anemia 1
|
|
Anemia Hypochromic
|
X Chromosome-Linked Sideroblastic Anemia
|
|
Sideroblastic Anaemia 1
|
X-Linked Sideroblastic Anaemia
|
|
Anemia Hereditary Sideroblastic
|
Anemia Sex-Linked Hypochromic Sideroblastic
|
|
Congenital Sideroblastic Anemia
|
Sideroblastic Anemia X-Linked
|
|
Anemia, Sex-Linked Hypochromic Sideroblastic
|
Congenital Sideroblastic Anaemia
|
|
X-Linked Pyridoxine-Responsive Sideroblastic Anemia
|
Anemia Congenital Sideroblastic
|
|
Anemia, Sideroblastic, Type 1
|
Sex-Linked Hypochromic Sideroblastic Anaemia
|
|
Autosomal Recessive Sideroblastic Anaemia
|
Familial Sex Linked Hypochromic Anaemia
|
|
|
| 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]
|
|
|
| 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
|
|
|
| Ehrlichiosis |
|
Human Ehrlichiosis
|
He
|
|
Hey
|
|
|
| Erythroleukemia |
|
|
| Friedreich Ataxia |
|
Friedreich Ataxia 1
|
FRDA
|
|
Friedreich Ataxia With Retained Reflexes
|
Frda1
|
|
Fa
|
Friedreich'S Ataxia
|
|
Hereditary Spinal Ataxia
|
Fa1
|
|
Friedreich'S Tabes
|
Hereditary Spinal Sclerosis
|
|
Spinocerebellar Ataxia, Friedreich
|
Friedreich Spinocerebellar Ataxia
|
|
Friedrich'S Ataxia
|
|
|
| Restless Legs Syndrome |
|
Wed
|
Willis-Ekbom Disease
|
|
Restless Leg Syndrome
|
Ekbom Syndrome
|
|
Wittmaack-Ekbom Syndrome
|
Willis Ekbom Disease
|
|
Ekbom'S Syndrome
|
Rls
|
|
Restless Legs
|
Restless Legs Syndrome, Susceptibility To
|
|
|
| Polycythemia |
|
Erythrocythemia
|
Polycythemia Vera
|
|
Polycythaemia Due To High Altitude
|
|
|
| Human Granulocytic Anaplasmosis |
|
Human Granulocytic Ehrlichiosis
|
Hge
|
|
Human Ehrlichial Infection, Human Granulocytic Type
|
Human Anaplasmosis Due To Anaplasma Phagocytophilum
|
|
|
| Diphtheria |
|
Corynebacterium Infections
|
Corynebacterium Infection
|
|
Diphtherial Infection
|
Infection Due To Corynebacterium Diphtheriae
|
|
|
| Gastric Adenosquamous Carcinoma |
|
Adenosquamous Carcinoma Of Stomach
|
|
|
| Rheumatoid Arthritis |
|
RA
|
Arthritis, Rheumatoid
|
|
Rheumatoid Arthritis, Susceptibility To
|
Arthritis Or Polyarthritis, Rheumatic
|
|
Atrophic Arthritis
|
Rheumatism Arthritis
|
|
Rheumatoid Polyarthritis
|
|
|
| Alpha-Thalassemia |
|
Alpha Thalassemia
|
Alpha Thalassaemia
|
|
Alpha Plus Thalassemia
|
Thalassemia, Alpha-
|
|
Thalassemias, Alpha-
|
A-Thalassemia
|
|
Α-Thalassemia
|
A-THAL
|
|
Thalassemia
|
Alpha Thalassaemia Syndrome
|
|
|
| Malaria |
|
Malaria, Susceptibility To
|
Malaria, Resistance To
|
|
Malaria, Cerebral
|
Cerebral Malaria
|
|
Malaria, Severe, Susceptibility To
|
Malaria, Severe, Resistance To
|
|
Malaria, Cerebral, Susceptibility To
|
Induced Malaria
|
|
Malaria, Vivax, Protection Against
|
Malaria, Severe
|
|
Malaria, Cerebral, Reduced Risk Of
|
Malaria, Protection Against
|
|
Resistance To Malaria Due To G6pd Deficiency
|
Malaria Due To G6pd Deficiency
|
|
Malarial Encephalitis
|
CM
|
|
Malaria Cerebral
|
Susceptibility To Malaria
|
|
Acute Pernicious Fever
|
Aestivo-Autumnal Fever
|
|
Aestivo Autumnal Malaria
|
Chagres Fever
|
|
Continued Malaria Fever
|
Estivo-Autumnal Fever
|
|
Estivo-Autumnal Malaria
|
Estivo-Autumnal Malarial Fever
|
|
Falciparum Fever
|
Malignant Tertian Fever
|
|
Malignant Tertian Malaria
|
Pernicious Intermittent Fever
|
|
Pernicious Malaria
|
Quotidian Malaria
|
|
Subtertian Fever
|
Subtertian Malaria Fever
|
|
Subtertian Malignant Tertian Malaria
|
Tropical Malaria
|
|
Algid Malaria
|
Bilious Haemoglobinuric Fever
|
|
Black Water Fever
|
Blackwater Fever
|
|
Malarial Blackwater Fever
|
Severe Malarial Falciparum
|
|
West African Fever
|
Malarial Haematinuria
|
|
Haemoglobinuric Fever
|
Haemoglobinuric Malaria
|
|
Severe Plasmodium Falciparum Malaria
|
Malarial Haemoglobinuria
|
|
Malarial Haematuria
|
Falciparum Malaria [Malignant Tertian]
|
|
Malaria Tropica
|
Malarial Shock
|
|
Chagres Virus Disease
|
Malignant Malaria
|
|
Mtm - [Malignant Tertian Malaria]
|
Tm -[Malignant Tertian Malaria]
|
|
Panama Fever
|
St - [Subtertian Malaria]
|
|
Malarial Quotidian
|
Benign Tertian Malaria
|
|
Tertian Ague
|
Vivax Fever
|
|
Plasmodium Vivax Malaria Nos
|
Btm - [Benign Tertian Malaria]
|
|
Bt - [Benign Tertian Malaria]
|
Vivax Malaria
|
|
Benign Tertian Vivax Malaria
|
Tertian Malaria
|
|
Quartan Malaria
|
Quartan Ague
|
|
Quartan Fever
|
Plasmodium Malariae Malaria Nos
|
|
Quartan Malarial
|
Malaria By Plasmodium Malariae
|
|
Malariae Malaria
|
Ovale Tertian Malaria
|
|
Plasmodium Ovale Fever
|
Malaria Fever By Plasmodium Ovale
|
|
Ovale Malaria
|
Malaria By Plasmodium Ovale
|
|
Malarial Ovale
|
Marsh Fever
|
|
Remittent Congestive Fever
|
Coastal Fever
|
|
Remittent Gastric Fever
|
Miasmatic Fever
|
|
Congestive Remittent Fever
|
Intermittent Fever
|
|
Jungle Fever
|
Paludism
|
|
Cameroon Fever
|
Ague
|
|
Corsican Fever
|
Intermittent Bilious Fever
|
|
Disease Due To Plasmodiidae
|
Malarial Fever
|
|
Plasmodiosis
|
Remittent Fever
|
|
Roman Fever
|
Malaria Fever Nos
|
|
Malaria Nos
|
Paludal Fever
|
|
Clinically Diagnosed Malaria
|
Clinically Diagnosed Malaria Without Parasitological Confirmation
|
|
Congestive Fever
|
Malarial Cachexia
|
|
Marsh Cachexia
|
Paludal Cachexia
|
|
Recurrent Malaria
|
Remittent Malaria
|
|
|
| Porphyria |
|
Hematoporphyria
|
Porphyrias
|
|
Disorder Of Porphyrin And Hem Metabolism
|
Disorder Of Porphyrin Metabolism
|
|
Porphyrinopathy
|
Porphyrin Disorder
|
|
Disorder Of Porphyrin And Heme Metabolism
|
Disorders Of Porphyrin Metabolism
|
|
|
| Brain Cancer |
|
Adult Brain Tumor
|
Malignant Neoplasm Of Brain
|
|
Brain Neoplasms
|
Brain Neoplasm
|
|
Neoplasm Of Brain
|
Primary Malignant Neoplasm Of Brain
|
|
Brain Tumors
|
Adult Malignant Brain Neoplasm
|
|
Brain Neoplasm, Adult
|
Bt - Brain Tumour
|
|
Malignant Brain Tumour
|
Malignant Primary Brain Neoplasm
|
|
Malignant Primary Brain Tumor
|
Malignant Tumor Of Adult Brain
|
|
Malignant Tumor Of Brain
|
Primary Brain Neoplasm
|
|
Primary Brain Tumor
|
Tumor Of The Brain
|
|
Brain Tumor, Adult
|
Brain Tumor Primary
|
|
Malignant Primary Brain Tumors
|
Primary Brain Tumors
|
|
Cancer, Brain
|
Brain Tumor, Primary
|
|
|
| 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
|
|
|
| Metal Metabolism Disorder |
|
Metal Metabolism, Inborn Errors
|
Inborn Metal Metabolism Disorder
|
|
|
| Hereditary Spherocytosis |
|
Congenital Spherocytic Hemolytic Anemia
|
Spherocytic Anemia
|
|
Congenital Spherocytosis
|
Spherocytosis, Type 1
|
|
Minkowski Chauffard Syndrome
|
Hs
|
|
Minkowski-Chauffard Disease
|
Minkowski-Chauffard Syndrome
|
|
Spherocytosis Hereditary
|
Spherocytosis, Hereditary
|
|
Anemia, Hereditary Spherocytic Hemolytic
|
|
|
| Sideroblastic Anemia |
|
Anemia Sideroblastic
|
Anemia, Sideroblastic
|
|
Anemia, Hypochromic With Iron Loading
|
|
|
| Bolivian Hemorrhagic Fever |
|
Machupo Hemorrhagic Fever
|
Hemorrhagic Fever, Bolivian
|
|
Bhf - [Bolivian Haemorrhagic Fever]
|
Machupo Haemorrhagic Fever
|
|
|
| Hemoglobinuria |
|
|
| Hemoglobinopathy |
|
|
| Anemia, Congenital Dyserythropoietic, Type Ia |
|
Congenital Dyserythropoietic Anemia Type I
|
Cda I
|
|
CDAN1A
|
Congenital Dyserythropoietic Anemia Type 1
|
|
Congenital Dyserythropoietic Anemia Type Ia
|
Congenital Dyserythropoietic Anemia, Type I
|
|
Anemia, Congenital Dyserythropoietic, Type I
|
Cda Type 1
|
|
Cda Type I
|
Cda Ia
|
|
Dyserythropoietic Anemia, Congenital Type 1
|
Anemia, Congenital Dyserythropoietic, Type 1a
|
|
Dyserythropoietic Anemia, Congenital, Type Ia
|
Cda, Type Ia
|
|
Congenital Dyserythropoietic Anaemia Type 1
|
Congenital Dyserythropoietic Anaemia Type I
|
|
Anemia, Dyserythropoietic, Congenital Type 1
|
Type I Congenital Dyserythropoietic Anemia
|
|
Anemia, Congenital Dyserythropoietic, 1a
|
Anemia, Dyserythropoietic, Congenital, Type Ia
|
|
|
| Hemochromatosis, Type 3 |
|
Hemochromatosis Type 3
|
HFE3
|
|
Hemochromatosis Due To Defect In Transferrin Receptor 2
|
Tfr2-Related Hemochromatosis
|
|
Tfr2-Related Hereditary Hemochromatosis
|
Hemochromatosis 3
|
|
|
| Iga Glomerulonephritis |
|
Iga Nephropathy
|
Glomerulonephritis, Iga
|
|
Berger'S Iga Or Igg Nephropathy
|
Focal Glomerulonephritis
|
|
Primary Iga Nephropathy
|
Segmental Glomerulonephritis
|
|
Berger Disease
|
Berger'S Disease
|
|
Igan
|
Nephritis, Iga Type
|
|
Nephropathy Iga
|
Glomerulonephritis Focal
|
|
Iga Nephropathy, Susceptibility To
|
Primary Immunoglobulin A Nephropathy
|
|
|
| Argentine Hemorrhagic Fever |
|
Argentinian Hemorrhagic Fever
|
Junin Hemorrhagic Fever
|
|
Hemorrhagic Fever, Argentinian
|
Ahf - [Argentinian Haemorrhagic Fever]
|
|
Argentine Haemorrhagic Fever
|
Junin Haemorrhagic Fever
|
|
|
| Brain Edema |
|
Cerebral Edema
|
Intracranial Swelling
|
|
Wet Brain
|
|
|
| Atransferrinemia |
|
Familial Hypotransferrinemia
|
Congenital Atransferrinemia
|
|
Hypotransferrinemia, Familial
|
Congenital Hypotransferrinemia
|
|
ATRAF
|
|
|
| Arthritis |
|
Inflammatory Joint Disease
|
Inflammatory Disorder Of Joint
|
|
|
| Myelodysplastic Syndrome |
|
Myelodysplastic Syndromes
|
Myelodysplasia
|
|
MDS
|
Myelodysplastic Syndrome Included
|
|
Myelodysplastic Syndrome, Susceptibility To, Included
|
Myelodysplastic Syndrome, Somatic
|
|
Myelodysplastic Syndrome, Susceptibility To
|
|
|
| Hemochromatosis Type 2 |
|
Juvenile Hemochromatosis
|
Juvenile Hereditary Hemochromatosis
|
|
Hfe2
|
Jhh
|
|
Hemochromatosis Juvenile
|
Iron Overload Disease Juvenile
|
|
Hemochromatosis, Juvenile
|
Hemochromatosis, Type 2
|
|
Hemochromatosis
|
Hemochromatosis, Type 1
|
|
|
| Neutropenia |
|
|
| Acute Erythroid Leukemia |
|
Acute Erythroleukemia
|
Di Guglielmo'S Syndrome
|
|
Aml M6
|
Acute Myeloid Leukemia Fab-M6
|
|
Acute Myeloid Leukemia M6
|
Erythroleukemia
|
|
Aml-M6
|
Acute Erythroleukemia M6a Subtype
|
|
Acute Erythroleukemia M6b Subtype
|
Di Guglielmo Syndrome
|
|
Acute Myeloid Leukemia, M6 Type
|
Acute Erythroblastic Leukemia
|
|
Acute Erythroleukemia - M6a Subtype
|
Acute Erythroleukemia - M6b Subtype
|
|
Acute Erythraemia And Erythroleukaemia
|
Acute Erythroid Leukaemia Without Mention Of Remission
|
|
Erythraemia
|
Erythraemic Myelosis
|
|
Erythroleukaemia
|
Acute Erythraemic Myelosis
|
|
Acute Erythraemia
|
|
|
| Megaloblastic Anemia |
|
Imerslund-Grasbeck Syndrome
|
Igs
|
|
Defect Of Enterocyte Intrinsic Factor Receptor
|
Enterocyte Cobalamin Malabsorption
|
|
Familial Megaloblastic Anemia
|
Megaloblastic Anemia 1
|
|
Selective Cobalamin Malabsorption With Proteinuria
|
Imerslund-Gräsbeck Syndrome
|
|
Anemia, Megaloblastic
|
Grasbeck-Imerslund Syndrome
|
|
Megaloblastic Anaemia
|
Mga1 Norwegian Type
|
|
Recessive Hereditary Megaloblastic Anaemia 1
|
Recessive Hereditary Megaloblastic Anemia 1
|
|
Rh-Mga1
|
Gräsbeck-Imerslund Disease
|
|
Pernicious Anemia, Juvenile, Due To Selective Intestinal Malabsorption Of Vitamin B12, With Proteinuria
|
Juvenile Pernicious Anemia With Proteinuria Due To Selective Intestinal Malabsorption Of Vitamin B12
|
|
Anemia Megaloblastic
|
Megaloblastic Anemia Due To Inborn Errors Of Metabolism
|
|
3-@Methylglutaconic Aciduria, Type I
|
|
|
| Hypochromic Microcytic Anemia |
|
Anemia, Hypochromic Microcytic
|
Microcytic Hypochromic Anemia
|
|
|
| Polycythemia Vera |
|
PV
|
Polycythemia Rubra Vera
|
|
Prv
|
Osler-Vaquez Disease
|
|
Chronic Erythremia
|
Polycythaemia Rubra Vera
|
|
Primary Polycythemia
|
Vaquez Disease
|
|
Polycythemia Vera, Somatic
|
Osler-Vaquez Syndrome
|
|
Proliferative Polycythaemia
|
Polycythemia Ruba Vera
|
|
Acquired Primary Erythrocytosis
|
Heilmeyer-Schoner Disease
|
|
Vaquez Osler Disease
|
Primary Polycythaemia
|
|
|
| Celiac Disease 1 |
|
Celiac Disease
|
Coeliac Disease
|
|
Celiac Sprue
|
Celiac Disease, Susceptibility To
|
|
Gluten-Sensitive Enteropathy
|
Nontropical Sprue
|
|
Sprue
|
CELIAC1
|
|
Celiac Disease, Susceptibility To, 1
|
Celiac Sprue 1
|
|
Celiac Sprue, Susceptibility To, 1
|
Gluten-Sensitive Enteropathy 1
|
|
Gluten-Sensitive Enteropathy, Susceptibility To, 1
|
Idiopathic Steatorrhea
|
|
Cœliac Disease
|
Gluten Intolerance
|
|
Gluten-Induced Enteropathy
|
Gluten Enteropathy
|
|
Celiac Disease, Susceptibility To, Type 1
|
Childhood Celiac Disease
|
|
Coeliac Rickets
|
Gee Disease
|
|
Gee-Herter Disease
|
Heubner-Herter Disease
|
|
Idiopathic Steatorrhoea
|
Thaysen'S Disease
|
|
Herter Gee Syndrome
|
|
|
| Hemochromatosis, Type 4 |
|
Hemochromatosis Type 4
|
Hemochromatosis Due To Defect In Ferroportin
|
|
HFE4
|
Hemochromatosis, Autosomal Dominant
|
|
Autosomal Dominant Hereditary Hemochromatosis
|
Ferroportin Disease
|
|
Hemochromatosis 4
|
Hemochromatosis Autosomal Dominant
|
|
|
| Beta-Thalassemia Intermedia |
|
|
| Brazilian Hemorrhagic Fever |
|
|
| Nutritional Deficiency Disease |
|
Malnutrition
|
Nutritional Disorder
|
|
Nutritional Deficiency
|
Nutrition
|
|
Deficiency Diseases
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
|
Nutrition Disorders
|
|
|
| Dysgerminoma |
|
|
| Beta-Thalassemia Major |
|
Cooley'S Anemia
|
Cooley Anemia
|
|
Mediterranean Anemia
|
|
|
| Anemia Of Prematurity |
|
|
| Plasmodium Vivax Malaria |
|
Malaria, Vivax
|
Malaria By Plasmodium Vivax
|
|
Vivax Malaria
|
Malaria Vivax
|
|
|
| Disease By Infectious Agent |
|
Infectious Disease
|
Infectious Diseases
|
|
|
| Mucopolysaccharidosis, Type Ii |
|
Hunter Syndrome
|
Iduronate 2-Sulfatase Deficiency
|
|
Mucopolysaccharidosis Ii
|
Mps Ii
|
|
Mucopolysaccharidosis Type Ii
|
MPS2
|
|
Sulfoiduronate Sulfatase Deficiency
|
Mucopolysaccharidosis, Mps-Ii
|
|
Ids Deficiency
|
Sids Deficiency
|
|
I2s Deficiency
|
Mucopolysaccharidosis Type 2
|
|
Mucopolysaccharidosis Type 2, Severe Form
|
Deficiency Of Iduronate-2-Sulphatase
|
|
Hunter'S Syndrome
|
Mps Ii - Hunter Syndrome
|
|
Iduronate-2-Sulfatase Deficiency
|
Attenuated Mps
|
|
Mps 2
|
Severe Mps Ii
|
|
Mpsii
|
Mucopolysaccharidosis Type 2, Attenuated Form
|
|
Hunter Syndrome Type B
|
Iduronate 2-Sulfatase Deficiency Type B
|
|
Mps2b
|
Mpsiib
|
|
Mucopolysaccharidosis Type 2b
|
Mucopolysaccharidosis Type Ii, Attenuated Form
|
|
Mucopolysaccharidosis Type Iib
|
Hunter Syndrome Type A
|
|
Iduronate 2-Sulfatase Deficiency Type A
|
Mps2a
|
|
Mpsiia
|
Mucopolysaccharidosis Type 2a
|
|
Mucopolysaccharidosis Type Ii, Severe Form
|
Mucopolysaccharidosis Type Iia
|
|
Mucopolysaccharidosis 2
|
Hunters Syndrome
|
|
Iduronate 2-Sulphatase Deficiency
|
Iduronate Sulfatase Deficiency
|
|
Iduronate Sulphatase Deficiency
|
Sulfo-Iduronate Sulfatase Deficiency
|
|
Sulfoiduronidate Sulfatase Deficiency
|
Sulpho-Iduronate Sulphatase Deficiency
|
|
Sulphoiduronidate Sulphatase Deficiency
|
Mps2 - [Mucopolysaccharidosis 2]
|
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Neonatal Anemia |
|
Anemia Neonatal
|
Anemia, Neonatal
|
|
Anaemia Neonatal
|
Neonatal Anaemia
|
|
|
| Human Immunodeficiency Virus Type 1 |
|
Aids
|
Hiv/Aids
|
|
Aids, Delayed/Rapid Progression To
|
Hiv-1, Susceptibility To
|
|
Hiv-1 Viremia, Susceptibility To
|
Human Immunodeficiency Virus Type 1, Susceptibility To
|
|
Hiv-1
|
Aids, Slow Progression To
|
|
Rapid Progression To Aids From Hiv1 Infection
|
Hiv1 Infection, Resistance To
|
|
Hiv1 Infection
|
Hiv-1 Viremia
|
|
Aids, Resistance To
|
Aids, Rapid Progression To
|
|
Hiv/Aids, Susceptibility To
|
Hiv-1, Resistance To
|
|
Hiv1, Resistance To
|
Hiv1
|
|
Hiv-1 Disease, Delayed Progression Of
|
Hiv-1 Disease, Rapid Progression Of
|
|
Hiv Infection, Resistance To
|
Hiv Type 1, Susceptibility To
|
|
Hiv Type 1
|
Hiv-1 Infection
|
|
Human Immunodeficiency Virus I Infection
|
Acquired Immunodeficiency Syndrome
|
|
Hiv-Infection/Aids
|
|
|
| Nephrotic Syndrome |
|
Finnish Congenital Nephrotic Syndrome
|
Ns - [Nephrotic Syndrome]
|
|
Nephrosis Syndrome
|
Nephrosis Nos
|
|
Glomerular Lesion Nephrosis
|
|
|
| Hemosiderosis |
|
Haemosiderosis
|
Iron Overload
|
|
|
| Lymphoma, Non-Hodgkin, Familial |
|
Non-Hodgkin Lymphoma
|
Lymphoma, Non-Hodgkin
|
|
NHL
|
Lymphoma, Non-Hodgkin, Somatic
|
|
Lymphoma, Follicular, Somatic
|
Familial Non-Hodgkin Lymphoma
|
|
Lymphoma Non-Hodgkins
|
Follicular Lymphoma, Somatic
|
|
Lymphosarcoma
|
Non-Hodgkins Lymphoma
|
|
|
| Gliosarcoma |
|
Glioblastoma With Sarcomatous Component
|
Sarcomatous Glioblastoma
|
|
|
| Congenital Hemolytic Anemia |
|
Anemia Hemolytic Congenital
|
Anemia, Hemolytic, Congenital
|
|
Congenital Hemolytic Anaemia
|
Hereditary Hemolytic Anaemia
|
|
Hereditary Hemolytic Anemia
|
|
|
| Occlusion Of Gallbladder |
|
Obstruction Of Gallbladder
|
Gallbladder Obstruction
|
|
|
| Hemoglobin E Disease |
|
Hemoglobin E
|
Hb-E Disease
|
|
|
| Sickle Cell Anemia |
|
Hemoglobin Sc Disease
|
Anemia, Sickle Cell
|
|
Hbsc Disease
|
Sickle Cell-Hemoglobin C Disease Syndrome
|
|
Hb Ss Disease
|
Sickle Cell Trait
|
|
Drepanocytosis
|
Haemoglobin Sc Disease
|
|
Hb Sc Disease
|
Hb-S/Hb-C Disease
|
|
Hb-Ss Disease Without Crisis
|
Hemoglobin S Disease Without Crisis
|
|
Sickle Cell Anaemia
|
Sickle-Cell/Hb-C Disease Without Crisis
|
|
Sickle Cell - Hemoglobin C Disease
|
Hbs Disease
|
|
Hemoglobin S Disease
|
Sickling Disorder Due To Hemoglobin S
|
|
SKCA
|
Sickle Cell Disease
|
|
Sickle Cell-Hemoglobin C Disease
|
Sickle-Cell Disease Carrier
|
|
Sickle-Cell Heterozygous Disorder
|
Haemoglobin A-S Genotype
|
|
Hb-S - [Sickle Cell Haemoglobin] Carrier
|
Sickle Cell Haemoglobin Trait
|
|
As - [Sickle Cell Trait]
|
Hbas - [Sickle Cell Haemoglobin Trait]
|
|
Sickle-Cell Trait Haemoglobin Disease
|
Haemoglobin Sickle Cell Trait Disorder
|
|
Heterozygous Sickle Cell Trait
|
Hbas - [Heterozygous Haemoglobin S]
|
|
|
| Aplastic Anemia |
|
Aplastic Anemia, Susceptibility To
|
Anemia Aplastic
|
|
Idiopathic Aplastic Anemia
|
Secondary Aplastic Anemia
|
|
Idiopathic Bone Marrow Failure
|
Aplastic Anemia Idiopathic
|
|
AA
|
Anemia, Aplastic
|
|
Aplastic Anemia, Idiopathic
|
Erythroid Aplasia
|
|
Aa - [Aplastic Anaemia]
|
Haematopoietic Aplasia
|
|
Aleukia Haemorrhagica
|
Anaemia Due To Decreased Red Cell Production
|
|
Aplasia Bone Marrow
|
Aplastic Bone Marrow
|
|
Hypoplastic Anaemia Nos
|
Myeloid Bone Marrow Aplasia
|
|
Pancytopenia
|
Panhaematopenia
|
|
Hypoproliferative Anaemia
|
Medullary Hypoplasia
|
|
Red Blood Cells Hypoplastic Anaemia
|
Panmyelophthisis
|
|
Panhemocytopenia
|
Refractive Hypoproliferative Anaemia
|
|
Toxic Anaemia
|
Toxic Aplastic Anaemia
|
|
Aplastic Anaemia Due To Toxic Cause
|
Idiopathic Aplastic Anaemia Nos
|
|
|
| Retinal Degeneration |
|
|
| Multiple Sclerosis |
|
MS
|
Multiple Sclerosis, Susceptibility To
|
|
Disseminated Sclerosis
|
Multiple Sclerosis, Disease Progression, Modifier Of
|
|
Insular Sclerosis
|
Multiple Sclerosis Modifier Of Disease Progression
|
|
Multiple Sclerosis, Susceptibility To 1
|
Multiple Sclerosis, Susceptibility To, 1
|
|
Multiple Sclerosis 1
|
Generalized Multiple Sclerosis
|
|
Multiple Sclerosis Variant
|
Multiple Sclerosis Susceptibility To
|
|
Cerebrospinal Sclerosis
|
Generalised Multiple Sclerosis
|
|
Ms - [Multiple Sclerosis]
|
Disseminated Cerebrospinal Sclerosis
|
|
Disseminated Multiple Sclerosis
|
Disseminated Nervous System Myelosclerosis
|
|
Multiple Cerebrospinal Sclerosis
|
Multiple Combined Sclerosis
|
|
Multiple Sclerosis Generalised
|
Disseminated Brain Sclerosis
|
|
Disseminated Spinal Sclerosis
|
Insular Brain Sclerosis
|
|
Miliary Brain Sclerosis
|
Multiple Combined Sclerosis Of Spinal Cord
|
|
Multiple Ascending Sclerosis
|
Multiple Brain Sclerosis
|
|
Multiple Sclerosis Of Brain Stem
|
Multiple Sclerosis Of The Brain Stem
|
|
Multiple Sclerosis Of Cord
|
Sclérose En Plaques
|
|
Plaque Sclerosis
|
Multiple Sclerosis Of The Spinal Cord
|
|
|
| Hemoglobin H Disease |
|
HBH
|
Hemoglobin H Disease, Nondeletional
|
|
Hemoglobin H Disease, Deletional
|
Alpha-Thalassemia Intermedia
|
|
Haemoglobin H Disease
|
Alpha-Thalassemia, Hemoglobin H Type
|
|
Hemoglobin H Disease, Deletional And Nondeletional
|
Alpha Thalassemia, Haemoglobin H Type
|
|
Alpha Thalassemia, Hemoglobin H Type
|
Haemoglobin H Disease, Deletional
|
|
Hbh Disease
|
Alpha-Thalassemia Hemoglobin H Type
|
|
Hemoglobin H Disease Deletional
|
Hemoglobin H Disease Non-Deletional
|
|
Alpha-Thalassemia
|
Alpha - /- - Or Mutational Forms Of Alpha-Thalassaemia
|
|
Alpha Thalassaemia Intermedia
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| Congenital Hypothyroidism |
|
Cretinism
|
Neonatal Hypothyroidism
|
|
Ch
|
Cht
|
|
Congenital Myxedema
|
Myxedema, Congenital
|
|
Endemic Cretinism
|
Congenital Iodine-Deficiency Syndrome
|
|
Fetal Iodine Deficiency Syndrome
|
Congenital Iodine-Deficiency Hypothyroidism Nos
|
|
|
| Parasitic Protozoa Infectious Disease |
|
Protozoan Infections
|
Mastigophora Infectious Disease
|
|
Sarcomastigophora Infectious Disease
|
|
|
| Ovarian Cancer |
|
Ovarian Carcinoma
|
Ovarian Neoplasm
|
|
Malignant Tumour Of Ovary
|
Cancer Of The Ovary
|
|
Epithelial Ovarian Cancer
|
Neoplasm Of Ovary
|
|
Ovarian Neoplasms
|
Ovarian Cancers
|
|
Malignant Neoplasm Of Ovary
|
Primary Malignant Neoplasm Of Ovary
|
|
Ovarian Cancer, Somatic
|
Malignant Ovarian Tumor
|
|
Ovary Neoplasm
|
Primary Ovarian Cancer
|
|
Tumor Of The Ovary
|
Malignant Neoplasm Of The Ovary
|
|
Malignant Tumor Of The Ovary
|
Ovarian Malignant Tumor
|
|
OC
|
Ovarian Carcinomas
|
|
Cancer, Ovarian
|
Cancer Of Ovary
|
|
Ovary Cancer
|
Ca Ovary
|
|
|
| Systemic Lupus Erythematosus |
|
Lupus Nephritis
|
SLE
|
|
Disseminated Lupus Erythematosus
|
Systemic Lupus Erythematosus, Susceptibility To
|
|
Lupus Erythematosus, Systemic
|
Lupus Nephritis, Susceptibility To
|
|
Libman-Sacks Disease
|
Systemic Lupus Erythematosus Susceptibility To
|
|
Sle - Lupus Erythematosus, Systemic
|
Le Syndrome
|
|
Lupus
|
Lupus Erythematosus Systemic
|
|
Lupus Erythematosus, Systemic, Susceptibility To
|
Lupus Vulgaris
|
|
Lupus Erythematosus, Discoid
|
Lupus Erythematosus
|
|
Systemic Lupus Erythematosus Nos
|
Sle - [Systemic Lupus Erythematosus]
|
|
|
| Spastic Paraplegia 38, Autosomal Dominant |
|
SPG38
|
Hereditary Spastic Paraplegia 38
|
|
Autosomal Dominant Spastic Paraplegia Type 38
|
Autosomal Dominant Spastic Paraplegia 38
|
|
|
| Neurodegeneration With Brain Iron Accumulation |
|
Nbia
|
Neurodegeneration With Brain Iron Accumulation Disorders
|
|
Neurodegeneration, With Brain Iron Accumulation
|
|
|
| T-Cell Acute Lymphoblastic Leukemia |
|
T-Cell Leukemia
|
Acute T Cell Leukemia
|
|
Precursor T Lymphoblastic Leukemia
|
Precursor T-Lymphoblastic Lymphoma/Leukemia
|
|
T Acute Lymphoblastic Leukemia
|
T-Cell Acute Lymphocytic Leukaemia
|
|
T-Cell Lymphoblastic Leukemia/Lymphoma
|
Leukemia T-Cell
|
|
Leukemia, T-Cell
|
Leukemia, Acute, Lymphoblastic, T-Cell
|
|
Leukemia, T-Cell Acute Lymphoblastic
|
Leukemia, Acute T-Cell
|
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
Precursor T-Cell Lymphoblastic Lymphoma
|
|
Precursor T Cell Lymphoblastic Leukemia/Lymphoblastic Lymphoma
|
|
|
| Aceruloplasminemia |
|
Cerebellar Ataxia
|
Hypoceruloplasminemia
|
|
Hemosiderosis, Systemic, Due To Aceruloplasminemia
|
Familial Apoceruloplasmin Deficiency
|
|
Hereditary Ceruloplasmin Deficiency
|
Deficiency Of Ferroxidase
|
|
Hypoceruloplasminemia, Hereditary
|
Ceruloplasmin Deficiency
|
|
Systemic Hemosiderosis Due To Aceruloplasminemia
|
ACERULOP
|
|
|
| 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
|
|
|
| Subacute Leukemia |
|
|
| Psychotic Disorder |
|
Psychotic Disorders
|
Mental Or Behavioural Disorder
|
|
Psychotic
|
Mental Disorders
|
|
|
| Flying Phobia |
|
|
| Leukemia, Chronic Lymphocytic |
|
Chronic Lymphocytic Leukemia
|
B-Cell Chronic Lymphocytic Leukemia
|
|
CLL
|
B-Cell Chronic Lymphoid Leukemia
|
|
Chronic Lymphatic Leukemia
|
Chronic Lymphocytic Leukaemia
|
|
Lymphoplasmacytic Leukemia
|
Small Lymphocytic Lymphoma
|
|
Leukemia, Chronic Lymphatic
|
B-Cell Chronic Lymphocytic Leukaemia
|
|
Chronic Lymphatic Leukaemia
|
Lymphoplasmacytic Leukaemia
|
|
B Cell Chronic Lymphocytic Leukemia
|
Chronic B-Cell Lymphocytic Leukemia
|
|
Leukemia, Lymphocytic, Chronic
|
B-Cll
|
|
Chronic Lymphoid Leukemia
|
Leukemia Lymphocytic Chronic
|
|
Lymphoma Small Lymphocytic
|
Leukemia, Lymphocytic, Chronic, B-Cell
|
|
|
| Immune Deficiency Disease |
|
Immunodeficiency
|
Primary Immunodeficiency
|
|
Primary Immunodeficiency Disease
|
Immunologic Deficiency Syndromes
|
|
Hypoimmunity
|
Immune Deficiency Disorder
|
|
Immunodeficiency Syndrome
|
Immune Disorder
|
|
Primary Immune Deficiency Disorder
|
Immune System Diseases
|
|
Human Immunodeficiency Virus Infection
|
Hiv - [Human Immunodeficiency Virus Infection]
|
|
Hiv Positive Nos
|
Hiv Disease
|
|
Acquired Immune Deficiency Syndrome-Related Complex
|
Aids-Like Syndrome
|
|
Aids-Related Complex Nos
|
Arc - [Aids-Related Complex]
|
|
Immunodeficiency Due To Human Immunodeficiency Virus Infection
|
Unspecified Human Immunodeficiency Virus Disease
|
|
Hiv Disease Nos
|
Human Immunodeficiency Virus Positive Nos
|
|
Hiv Nos
|
Deficiency Of Complement Initial Pathway
|
|
Deficiency Of Complement Terminal Pathway
|
Cfdd - [Complement Factor D Deficiency]
|
|
Immunodeficiency With Nk-Cell - [Natural-Killer Cell] Deficiency
|
Nonfamilial Hypogammaglobulinaemia
|
|
Common Variable Immune Deficiency
|
Nonfamilial Agammaglobulinaemia
|
|
Common Variable Agammaglobulinaemia
|
Agammaglobulinaemia Nos
|
|
Agammaglobulinaemia Antibody Deficiency Syndrome
|
Hypogammaglobulinaemia Antibody Deficiency Syndrome
|
|
Acquired Agammaglobulinaemia Nos
|
Hypogammaglobulinaemia Nos
|
|
Hyper Igm
|
|
|
| Breast Cancer |
|
Breast Carcinoma
|
Male Breast Cancer
|
|
Breast Cancer, Familial
|
Malignant Neoplasm Of Breast
|
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
|
Mammary Cancer
|
Mammary Tumor
|
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
|
Familial Breast Cancer
|
Cancer Of Breast
|
|
BC
|
Breast Cancer Familial
|
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
|
Breast Male Carcinoma
|
Breast Neoplasms
|
|
Breast Neoplasms, Male
|
Mammary Tumors
|
|
Mammary Carcinomas
|
Cancer, Breast
|
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
|
Carcinoma With Apocrine Differentiation
|
|
|
| Myeloma, Multiple |
|
Multiple Myeloma
|
Plasma Cell Myeloma
|
|
Kahler Disease
|
Myelomatosis
|
|
Medullary Plasmacytoma
|
Multiple Myeloma, Resistance To
|
|
Myeloma
|
Plasma Cell Dyscrasia
|
|
Kahler'S Disease
|
Multiple Myeloma, Susceptibility To
|
|
Myeloma - Multiple
|
Kahler-Bozzolo Disease
|
|
Plasma Cell Myelomas
|
MM
|
|
Plasma Cell Neoplasm
|
Primary Systemic Amyloidosis
|
|
Primary Amyloidosis
|
Immunoglobulin Deposition Disease
|
|
Plasmacytic Myeloma
|
Multiple Myelomata
|
|
Multiple Myeloma Nos
|
Multiple Myeloma Without Mention Of Remission
|
|
Monostotic Plasma Cell Myeloma
|
Mm - [Multiple Myeloma]
|
|
|
| Diamond-Blackfan Anemia |
|
Congenital Pure Red Cell Aplasia
|
Aase Syndrome
|
|
Erythrogenesis Imperfecta
|
Anemia, Diamond-Blackfan
|
|
Congenital Hypoplastic Anemia
|
Aase-Smith Ii Syndrome
|
|
Bds
|
Blackfan-Diamond Anemia
|
|
Congenital Prca
|
Congenital Hypoplastic Anemia, Blackfan-Diamond Type
|
|
Dba
|
Blackfan - Diamond Syndrome
|
|
Chronic Constitutional Pure Red Cell Anaemia
|
Anemia Diamond Blackfan Type
|
|
Anemia Congenital Erythroid Hypoplastic
|
Aregenerative Anemia Chronic Congenital
|
|
Blackfan Diamond Syndrome
|
Red Cell Aplasia, Pure Hereditary
|
|
Aase-Smith Syndrome Ii
|
Bda
|
|
Blackfan Diamond Anemia
|
Blackfan-Diamond Disease
|
|
Blackfan-Diamond Syndrome
|
Chronic Congenital Agenerative Anemia
|
|
Congenital Erythroid Hypoplastic Anemia
|
Congenital Hypoplastic Anemia Of Blackfan And Diamond
|
|
Congenital Pure Red Cell Anemia
|
Hypoplastic Congenital Anemia
|
|
Inherited Erythroblastopenia
|
Pure Hereditary Red Cell Aplasia
|
|
Anemia, Hypoplastic, Congenital
|
Anemia Hypoplastic Congenital
|
|
Fanconi Anemia
|
Constitutional Aplastic Anemia
|
|
Diamond-Blackfan Anemia 1
|
Aase Smith Syndrome 2
|
|
Congenital Red Cell Aplasia
|
Red Cell Aplasia Of Infants
|
|
Pure Red Cell Aplasia Of Infants
|
Congenital Red Cell Aplastic Anaemia
|
|
Congenital Pure Red Cell Anaemia
|
Congenital Erythroid Hypoplasia
|
|
Pearson Marrow-Pancreas Syndrome
|
|
|
| Body Mass Index Quantitative Trait Locus 11 |
|
OBESITY
|
Obesity, Susceptibility To
|
|
Leanness, Inherited
|
Obesity, Susceptibility To, Bmiq11
|
|
Obesity, Mild, Early-Onset
|
Obesity, Association With
|
|
Obesity, Early-Onset, Susceptibility To
|
Obesity, Severe
|
|
Obesity, Severe, And Type Ii Diabetes
|
Obesity, Late-Onset
|
|
Obesity , Susceptibility To
|
BMIQ11
|
|
Obesity Bmiq11
|
Obesity, Early-Onset
|
|
Simple Obesity Nos
|
Excess Fat
|
|
Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified
|
Adiposis
|
|
|
| Leukemia, Acute Myeloid |
|
Acute Myeloid Leukemia
|
Leukemia, Acute Myelogenous
|
|
Acute Myelogenous Leukemia
|
AML
|
|
Leukemia, Acute Myeloid, Susceptibility To
|
Acute Myeloblastic Leukemia
|
|
Leukemia, Acute Myeloid, Reduced Survival In, Somatic
|
Acute Myeloid Leukaemia
|
|
Leukemia, Myelocytic, Acute
|
Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome
|
|
Secondary Aml
|
Acute Myelocytic Leukemia
|
|
Acute Myeloid Leukemia, Somatic
|
Leukemia, Acute Myeloid, Somatic
|
|
Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic
|
Acute Myeloblastic Leukaemia
|
|
Acute Myelogenous Leukaemia
|
Aml - Acute Myeloid Leukemia
|
|
Acute Myeloid Leukemia With Cebpa Somatic Mutations
|
Aml With Cebpa Somatic Mutations
|
|
Inherited Acute Myeloid Leukemia
|
Familial Aml
|
|
Inherited Aml
|
Pure Familial Aml
|
|
Pure Familial Acute Myeloid Leukemia
|
Secondary Acute Myeloid Leukemia
|
|
Therapy-Related Aml And Myelodysplastic Syndrome
|
Acute Myeloid Leukemia, Secondary
|
|
Acute Non-Lymphoblastic Leukemia
|
Acute Non-Lymphocytic Leukemia
|
|
Acute Biphenotypic Leukemia
|
Acute Undifferentiated Leukemia
|
|
Acute Myeloblastic Leukaemia With Multilineage Dysplasia
|
Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission
|
|
Acute Myeloid Leukaemia With Myelodysplasia-Related Features
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
