| Diseases |
Alias |
|
| Hemochromatosis, Type 2b |
|
Hemochromatosis Type 2b
|
HFE2B
|
|
Hemochromatosis 2b
|
|
|
| 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
|
|
|
| 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
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Iron Deficiency Anemia |
|
Iron-Deficiency Anemia
|
Fe Deficiency Anaemia
|
|
Ida - [Iron Deficiency Anemia]
|
Fe - [Iron] Deficiency Anemia Nos
|
|
|
| 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]
|
|
|
| Metal Metabolism Disorder |
|
Metal Metabolism, Inborn Errors
|
Inborn Metal Metabolism Disorder
|
|
|
| Rare Hereditary Hemochromatosis |
|
Iron Overload
|
Iron Overload Disease
|
|
Idiopathic Haemosiderosis
|
Hemosiderosis
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Beta-Thalassemia Intermedia |
|
|
| Atransferrinemia |
|
Familial Hypotransferrinemia
|
Congenital Atransferrinemia
|
|
Hypotransferrinemia, Familial
|
Congenital Hypotransferrinemia
|
|
ATRAF
|
|
|
| Sideroblastic Anemia |
|
Anemia Sideroblastic
|
Anemia, Sideroblastic
|
|
Anemia, Hypochromic With Iron Loading
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Hemochromatosis, Type 3 |
|
Hemochromatosis Type 3
|
HFE3
|
|
Hemochromatosis Due To Defect In Transferrin Receptor 2
|
Tfr2-Related Hemochromatosis
|
|
Tfr2-Related Hereditary Hemochromatosis
|
Hemochromatosis 3
|
|
|
| Folic Acid Deficiency Anemia |
|
Folate Deficiency Anaemia
|
Folic Acid Deficiency Anaemia
|
|
Folate Deficiency Anemia
|
Folate-Deficiency Anaemia
|
|
Folate-Deficiency Anemia
|
Folate-Deficient Megaloblastic Anaemia
|
|
Megaloblastic Anemia Due To Folate Deficiency
|
Anaemia Of Folate Deficiency
|
|
Folate Or Folic Acid Deficiency Anaemia Nos
|
Folic Acid Deficiency Anaemia Nos
|
|
Acquired Megaloblastic Anaemia Due To Nutritional Folate Deficiency
|
Dietary Folic Acid Deficiency Anaemia
|
|
Dietary Folate Deficiency Anaemia
|
Folate Deficiency Anaemia Due To Dietary Causes
|
|
Goat'S Milk Anaemia
|
Acquired Megaloblastic Anaemia Due To Folate Deficiency Secondary To Increased Requirement
|
|
Megaloblastic Anaemia Due To Increased Requirements Of Folate
|
Acquired Megaloblastic Anaemia Due To Folate Deficiency Secondary To Intestinal Disorders
|
|
Acquired Megaloblastic Anaemia Due To Decreased Intestinal Absorption Of Folate
|
Megaloblastic Anaemia Due To Decreased Intestinal Absorption Of Folate
|
|
|
| Anemia Of Prematurity |
|
|
| Polycythemia |
|
Erythrocythemia
|
Polycythemia Vera
|
|
Polycythaemia Due To High Altitude
|
|
|
| Beta-Thalassemia Major |
|
Cooley'S Anemia
|
Cooley Anemia
|
|
Mediterranean Anemia
|
|
|
| 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
|
|
|
| Arthropathy |
|
Ankylosis Of Ankle And Foot Joint
|
Ankylosis Of Forearm Joint
|
|
Ankylosis Of Hand Joint
|
Ankylosis Of Joint Of Ankle And/Or Foot
|
|
Ankylosis Of Joint Of Forearm
|
Ankylosis Of Joint Of Hand
|
|
Ankylosis Of Joint Of Lower Leg
|
Ankylosis Of Joint Of Multiple Sites
|
|
Ankylosis Of Joint Of Pelvic Region And Thigh
|
Ankylosis Of Joint Of Shoulder Region
|
|
Ankylosis Of Joint Of Upper Arm
|
Ankylosis Of Lower Leg Joint
|
|
Ankylosis Of Multiple Joints
|
Ankylosis Of Upper Arm Joint
|
|
Infectious Arthropathy
|
Joint Ankylosis Of The Ankle And Foot
|
|
Joint Ankylosis Of The Ankle And/Or Foot
|
Joint Ankylosis Of The Forearm
|
|
Joint Ankylosis Of The Hand
|
Joint Ankylosis Of The Lower Leg
|
|
Joint Ankylosis Of The Pelvic Region And Thigh
|
Joint Ankylosis Of The Shoulder Region
|
|
Joint Ankylosis Of The Upper Arm
|
Joint Diseases
|
|
Joint Disease
|
Arthropathy Associated With Infection
|
|
|
| Iron Overload In Africa |
|
African Iron Overload
|
Bantu Siderosis
|
|
African Hemochromatosis
|
Hereditary Iron Overload And African Americans
|
|
African Nutritional Hemochromatosis
|
African Siderosis
|
|
|
| Hypochromic Microcytic Anemia |
|
Anemia, Hypochromic Microcytic
|
Microcytic Hypochromic Anemia
|
|
|
| Alpha-1-Antitrypsin Deficiency |
|
Alpha 1-Antitrypsin Deficiency
|
Alpha-1 Antitrypsin Deficiency
|
|
Aat Deficiency
|
Aatd
|
|
A1ATD
|
Emphysema Due To Aat Deficiency
|
|
A1at Deficiency
|
Emphysema-Cirrhosis, Due To Aat Deficiency
|
|
Hemorrhagic Diathesis Due To Antithrombin Pittsburgh
|
Alpha-1 Antiprotease Deficiency
|
|
Alpha 1 Antitrypsin Deficiency
|
Aat
|
|
Alpha-1 Protease Inhibitor Deficiency
|
Alpha-1 Related Emphysema
|
|
Genetic Emphysema
|
Hereditary Pulmonary Emphysema
|
|
Inherited Emphysema
|
Alpha-1-Proteinase Inhibitor Deficiency
|
|
Alpha1-Antitrypsin Deficiency
|
Alpha-1-Antitrypsin Deficiency, Autosomal Recessive
|
|
Emphysema, Hereditary Pulmonary
|
Aatd - [Alpha-1-Antitrypsin] Deficiency
|
|
|
| Hemosiderosis |
|
Haemosiderosis
|
Iron Overload
|
|
|
| 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
|
|
|
| Iron Metabolism Disease |
|
Iron Deficiency
|
Iron Disorder
|
|
Iron Metabolism Disorders
|
Disorder Of Iron Metabolism
|
|
Iron
|
Fe Deficiency
|
|
Iron Storage Disease
|
Iron Storage Disorder
|
|
|
| Microcytic Anemia |
|
Iron-Refractory Iron Deficiency Anemia
|
|
|
| Nutritional Deficiency Disease |
|
Malnutrition
|
Nutritional Disorder
|
|
Nutritional Deficiency
|
Nutrition
|
|
Deficiency Diseases
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
|
Nutrition Disorders
|
|
|
| Thalassemia Minor |
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Neonatal Anemia |
|
Anemia Neonatal
|
Anemia, Neonatal
|
|
Anaemia Neonatal
|
Neonatal Anaemia
|
|
|
| Mineral Metabolism Disease |
|
Mineral Metabolism Disorder
|
Disorder Of Mineral Metabolism
|
|
|
| Congenital Dyserythropoietic Anemia |
|
Congenital Dyshaematopoietic Anaemia
|
Dyserythropoietic Anemia, Congenital
|
|
Cda
|
Anemia, Dyserythropoietic, Congenital
|
|
Anemia Dyserythropoietic Congenital
|
Cda - [Congenital Dyserythropoietic Anaemia]
|
|
Dyserythropoietic Dyshaematopoietic Congenital Anaemia
|
Dyshaematopoietic Anaemia
|
|
Dyserythropoietic Anaemia
|
|
|
| Acute Porphyria |
|
Porphyrias, Hepatic
|
Hepatic Porphyria
|
|
Porphyria Hepatic
|
Acute Intermittent Porphyria
|
|
|
| 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
|
|
|
| Congenital Hemolytic Anemia |
|
Anemia Hemolytic Congenital
|
Anemia, Hemolytic, Congenital
|
|
Congenital Hemolytic Anaemia
|
Hereditary Hemolytic Anaemia
|
|
Hereditary Hemolytic Anemia
|
|
|
| Hemoglobinopathy |
|
|
| Vitamin B12 Deficiency |
|
Cobalamin Deficiency
|
Hypocobalaminemia
|
|
Vitamin B 12 Deficiency
|
Cyanocobalamin Deficiency
|
|
Deficiency Of Vitamin B12
|
|
|
| Cutaneous Porphyria |
|
Porphyria, Erythropoietic
|
Erythropoietic Porphyria
|
|
|
| Vitamin Metabolic Disorder |
|
|
| Multicentric Castleman Disease |
|
Mcd
|
Multicentric Giant Lymph Node Hyperplasia
|
|
Plasmablastic Multicentric Castleman Disease
|
Pmcd
|
|
Idiopathic Multicentric Castleman Disease
|
Multi-Centric Castleman'S Disease
|
|
Idiopathic Multicentric Castleman'S Disease
|
Multicentric Plasma Cell Variant Of Castleman'S Disease
|
|
Hhv-8-Negative Multicentric Castleman Disease
|
Human Herpesvirus-8-Negative Multicentric Castleman Disease
|
|
|
| Erythrocytosis, Familial, 2 |
|
Chuvash Polycythemia
|
ECYT2
|
|
Familial Erythrocytosis 2
|
Autosomal Recessive Benign Erythrocytosis
|
|
Polycythemia, Vhl-Dependent
|
Chuvash Erythromatosis
|
|
Chuvash Type Polycythemia
|
Chuvash Erythrocytosis
|
|
Von Hippel-Lindau-Dependent Polycythemia
|
Polycythemia Chuvash Type
|
|
Vhl-Dependent Polycythemia
|
Erythrocytosis, Familial, Type 2
|
|
|
| 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]
|
|
|
| Lung Clear Cell Carcinoma |
|
|
| Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema |
|
Dehydrated Hereditary Stomatocytosis
|
Hereditary Xerocytosis
|
|
Xerocytosis, Hereditary
|
Pshk1
|
|
Pseudohyperkalemia Edinburgh
|
Dehydrated Hereditary Stomatocytosis With Or Without Pseudohyperkalemia And/Or Perinatal Edema
|
|
DHS1
|
Dhs
|
|
Hereditary Desiccytosis
|
Dehydrated Hereditary Stomatocytosis 1
|
|
Desiccytosis, Hereditary
|
Pseudohyperkalemia, Familial, 1, Due To Red Cell Leak
|
|
Pseudohyperkalemia Familial 1, Due To Red Cell Leak
|
Desiccytosis Hereditary
|
|
Xerocytosis Hereditary
|
Familial Pseudohyperkalemia 1 Due To Red Cell Leak
|
|
Stomatocytosis, Dehydrated, Hereditary, With/Without Pseudohyperkalemia And/Or Perinatal Edema
|
Xerocytosis
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Osteoporosis |
|
Postmenopausal Osteoporosis
|
Osteoporosis, Postmenopausal
|
|
Bone Mineral Density Quantitative Trait Locus
|
Bmnd
|
|
Osteoporosis, Involutional
|
Osteoporosis, Susceptibility To
|
|
Osteoporosis, Postmenopausal, Susceptibility
|
Bone Mineral Density Variation Qtl, Osteoporosis
|
|
OSTEOP
|
Involutional Osteoporosis
|
|
Senile Osteoporosis
|
Osteoporosis Postmenopausal
|
|
Bone Mineral Density, Quantitative Trait Locus
|
Osteoporosis, Senile
|
|
Idiopathic Osteoporosis
|
Bone Rarefaction Nos
|
|
Type 1 Osteoporosis
|
|
|
| Anemia, Congenital Dyserythropoietic, Type Ib |
|
CDAN1B
|
Congenital Dyserythropoietic Anemia Type Ib
|
|
Cda, Type Ib
|
Congenital Dyserythropoietic Anemia Type Type 1b
|
|
Dyserythropoietic Anemia, Congenital, Type Ib
|
Anemia, Congenital Dyserythropoietic, 1b
|
|
Cda Ib
|
Anemia, Dyserythropoietic, Congenital
|
|
Anemia, Dyserythropoietic, Congenital, Type Ib
|
|
|
| Autosomal Dominant Beta Thalassemia |
|
Inclusion Body Beta-Thalassemia
|
|
|
| Alpha-Thalassemia |
|
Alpha Thalassemia
|
Alpha Thalassaemia
|
|
Alpha Plus Thalassemia
|
Thalassemia, Alpha-
|
|
Thalassemias, Alpha-
|
A-Thalassemia
|
|
Α-Thalassemia
|
A-THAL
|
|
Thalassemia
|
Alpha Thalassaemia Syndrome
|
|
|
| Intracranial Cavernous Angioma |
|
Intracranial Cavernoma
|
Intracranial Cavernous Hemangioma
|
|
|
| Intracranial Structure Hemangioma |
|
Angioma Of Intracranial Structure
|
Hemangioma Of Intracranial Structure
|
|
Hemangioma Of Intracranial Structures
|
|
|
| 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
|
|
|
