疾病名称 |
别名 |
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Malaria |
Malaria, Susceptibility To
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Malaria, Resistance To
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Malaria, Cerebral
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Cerebral Malaria
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Malaria, Severe, Susceptibility To
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Malaria, Severe, Resistance To
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Malaria, Cerebral, Susceptibility To
|
Induced Malaria
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Malaria, Vivax, Protection Against
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Malaria, Severe
|
Malaria, Cerebral, Reduced Risk Of
|
Malaria, Protection Against
|
Resistance To Malaria Due To G6pd Deficiency
|
Malaria Due To G6pd Deficiency
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Malarial Encephalitis
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CM
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Malaria Cerebral
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Susceptibility To Malaria
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Acute Pernicious Fever
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Aestivo-Autumnal Fever
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Aestivo Autumnal Malaria
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Chagres Fever
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Continued Malaria Fever
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Estivo-Autumnal Fever
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Estivo-Autumnal Malaria
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Estivo-Autumnal Malarial Fever
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Falciparum Fever
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Malignant Tertian Fever
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Malignant Tertian Malaria
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Pernicious Intermittent Fever
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Pernicious Malaria
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Quotidian Malaria
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Subtertian Fever
|
Subtertian Malaria Fever
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Subtertian Malignant Tertian Malaria
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Tropical Malaria
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Algid Malaria
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Bilious Haemoglobinuric Fever
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Black Water Fever
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Blackwater Fever
|
Malarial Blackwater Fever
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Severe Malarial Falciparum
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West African Fever
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Malarial Haematinuria
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Haemoglobinuric Fever
|
Haemoglobinuric Malaria
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Severe Plasmodium Falciparum Malaria
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Malarial Haemoglobinuria
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Malarial Haematuria
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Falciparum Malaria [Malignant Tertian]
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Malaria Tropica
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Malarial Shock
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Chagres Virus Disease
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Malignant Malaria
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Mtm - [Malignant Tertian Malaria]
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Tm -[Malignant Tertian Malaria]
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Panama Fever
|
St - [Subtertian Malaria]
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Malarial Quotidian
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Benign Tertian Malaria
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Tertian Ague
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Vivax Fever
|
Plasmodium Vivax Malaria Nos
|
Btm - [Benign Tertian Malaria]
|
Bt - [Benign Tertian Malaria]
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Vivax Malaria
|
Benign Tertian Vivax Malaria
|
Tertian Malaria
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Quartan Malaria
|
Quartan Ague
|
Quartan Fever
|
Plasmodium Malariae Malaria Nos
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Quartan Malarial
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Malaria By Plasmodium Malariae
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Malariae Malaria
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Ovale Tertian Malaria
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Plasmodium Ovale Fever
|
Malaria Fever By Plasmodium Ovale
|
Ovale Malaria
|
Malaria By Plasmodium Ovale
|
Malarial Ovale
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Marsh Fever
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Remittent Congestive Fever
|
Coastal Fever
|
Remittent Gastric Fever
|
Miasmatic Fever
|
Congestive Remittent Fever
|
Intermittent Fever
|
Jungle Fever
|
Paludism
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Cameroon Fever
|
Ague
|
Corsican Fever
|
Intermittent Bilious Fever
|
Disease Due To Plasmodiidae
|
Malarial Fever
|
Plasmodiosis
|
Remittent Fever
|
Roman Fever
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Malaria Fever Nos
|
Malaria Nos
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Paludal Fever
|
Clinically Diagnosed Malaria
|
Clinically Diagnosed Malaria Without Parasitological Confirmation
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Congestive Fever
|
Malarial Cachexia
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Marsh Cachexia
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Paludal Cachexia
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Recurrent Malaria
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Remittent Malaria
|
|
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Hepatitis A |
Viral Hepatitis A
|
Viral Hepatitis, Type A
|
|
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Pyridoxine-Responsive Sideroblastic Anemia |
|
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Hereditary Spherocytosis |
Congenital Spherocytic Hemolytic Anemia
|
Spherocytic Anemia
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Congenital Spherocytosis
|
Spherocytosis, Type 1
|
Minkowski Chauffard Syndrome
|
Hs
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Minkowski-Chauffard Disease
|
Minkowski-Chauffard Syndrome
|
Spherocytosis Hereditary
|
Spherocytosis, Hereditary
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Anemia, Hereditary Spherocytic Hemolytic
|
|
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Anemia, Autoimmune Hemolytic |
Autoimmune Hemolytic Anemia
|
Idiopathic Autoimmune Hemolytic Anemia
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Immuno-Hemolytic Anemia
|
Anemia, Hemolytic, Autoimmune
|
Autoimmune Haemolytic Anaemia
|
Autoimmune Hemolytic Anaemia
|
Acquired Autoimmune Hemolytic Anemia
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Anemia Hemolytic Autoimmune
|
Familial Auto-Immune Hemolytic Anemia
|
Aha
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Aiha
|
|
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Gastric Teratoma |
|
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Acute Erythroid Leukemia |
Acute Erythroleukemia
|
Di Guglielmo'S Syndrome
|
Aml M6
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Acute Myeloid Leukemia Fab-M6
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Acute Myeloid Leukemia M6
|
Erythroleukemia
|
Aml-M6
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Acute Erythroleukemia M6a Subtype
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Acute Erythroleukemia M6b Subtype
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Di Guglielmo Syndrome
|
Acute Myeloid Leukemia, M6 Type
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Acute Erythroblastic Leukemia
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Acute Erythroleukemia - M6a Subtype
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Acute Erythroleukemia - M6b Subtype
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Acute Erythraemia And Erythroleukaemia
|
Acute Erythroid Leukaemia Without Mention Of Remission
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Erythraemia
|
Erythraemic Myelosis
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Erythroleukaemia
|
Acute Erythraemic Myelosis
|
Acute Erythraemia
|
|
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Malignant Gastric Germ Cell Tumor |
Germ Cell Tumor Of The Stomach
|
Germ Cell Tumour Of The Stomach
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Malignant Gastric Germ Cell Tumour
|
|
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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
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Chronic Constitutional Pure Red Cell Anaemia
|
Anemia Diamond Blackfan Type
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Anemia Congenital Erythroid Hypoplastic
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Aregenerative Anemia Chronic Congenital
|
Blackfan Diamond Syndrome
|
Red Cell Aplasia, Pure Hereditary
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Aase-Smith Syndrome Ii
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Bda
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Blackfan Diamond Anemia
|
Blackfan-Diamond Disease
|
Blackfan-Diamond Syndrome
|
Chronic Congenital Agenerative Anemia
|
Congenital Erythroid Hypoplastic Anemia
|
Congenital Hypoplastic Anemia Of Blackfan And Diamond
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Congenital Pure Red Cell Anemia
|
Hypoplastic Congenital Anemia
|
Inherited Erythroblastopenia
|
Pure Hereditary Red Cell Aplasia
|
Anemia, Hypoplastic, Congenital
|
Anemia Hypoplastic Congenital
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Fanconi Anemia
|
Constitutional Aplastic Anemia
|
Diamond-Blackfan Anemia 1
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Aase Smith Syndrome 2
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Congenital Red Cell Aplasia
|
Red Cell Aplasia Of Infants
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Pure Red Cell Aplasia Of Infants
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Congenital Red Cell Aplastic Anaemia
|
Congenital Pure Red Cell Anaemia
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Congenital Erythroid Hypoplasia
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Pearson Marrow-Pancreas Syndrome
|
|
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Anemia, Congenital Dyserythropoietic, Type Ia |
Congenital Dyserythropoietic Anemia Type I
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Cda I
|
CDAN1A
|
Congenital Dyserythropoietic Anemia Type 1
|
Congenital Dyserythropoietic Anemia Type Ia
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Congenital Dyserythropoietic Anemia, Type I
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Anemia, Congenital Dyserythropoietic, Type I
|
Cda Type 1
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Cda Type I
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Cda Ia
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Dyserythropoietic Anemia, Congenital Type 1
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Anemia, Congenital Dyserythropoietic, Type 1a
|
Dyserythropoietic Anemia, Congenital, Type Ia
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Cda, Type Ia
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Congenital Dyserythropoietic Anaemia Type 1
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Congenital Dyserythropoietic Anaemia Type I
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Anemia, Dyserythropoietic, Congenital Type 1
|
Type I Congenital Dyserythropoietic Anemia
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Anemia, Congenital Dyserythropoietic, 1a
|
Anemia, Dyserythropoietic, Congenital, Type Ia
|
|
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Carrion'S Disease |
Oroya Fever
|
Carrion Disease
|
Bartonellosis Due To Bartonella Bacilliformis Infection
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Bartonella Infections
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Systemic Bartonellosis Due To Bartonella Bacilliformis
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Systemic Carrión Disease
|
Systemic Bartonellosis
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Bartonella Fever
|
|
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Hereditary Elliptocytosis |
Congenital Elliptocytosis
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Ovalocytosis
|
Elliptocytosis, Hereditary
|
He
|
Elliptocytosis Hereditary
|
Congenital Ovalocytosis
|
Elliptocytosis
|
Hereditary Elliptocytosis With Infantile Poikilocytosis
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Hereditary Ovalocytosis
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Oval Erythrocytosis
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He - [Hereditary Elliptocytosis]
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Elliptocytosis Anaemia
|
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Duodenum Adenoma |
|
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Myelodysplastic Syndrome |
Myelodysplastic Syndromes
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Myelodysplasia
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MDS
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Myelodysplastic Syndrome Included
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Myelodysplastic Syndrome, Susceptibility To, Included
|
Myelodysplastic Syndrome, Somatic
|
Myelodysplastic Syndrome, Susceptibility To
|
|
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Fetal Erythroblastosis |
Erythroblastosis, Fetal
|
Ef - Erythroblastosis Foetalis
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Erythroblastosis Fetalis
|
Haemolytic Disease Due To Rhesus Isoimmunisation
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Rhesus Isoimmunisation Of The Newborn
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|
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Myasthenic Syndrome, Congenital, 3a, Slow-Channel |
Congenital Myasthenic Syndrome 3a
|
CMS3A
|
Congenital Myasthenic Syndrome 3a, Slow-Channel
|
Myasthenic Syndrome, Congenital, Type 3a, Slow-Channel
|
|
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Congenital Hemolytic Anemia |
Anemia Hemolytic Congenital
|
Anemia, Hemolytic, Congenital
|
Congenital Hemolytic Anaemia
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Hereditary Hemolytic Anaemia
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Hereditary Hemolytic Anemia
|
|
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Anemia Of Prematurity |
|
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Myeloproliferative Syndrome, Transient |
Transient Abnormal Myelopoiesis
|
Transient Myeloproliferative Syndrome
|
Transient Myeloproliferative Disease
|
Mst
|
Tam
|
Leukemia, Transient, Of Down Syndrome
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Tmd
|
Leukemia, Transient
|
Transient Leukemia
|
Transient Leukemia Of Down Syndrome
|
|
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Sickle Cell Anemia |
Hemoglobin Sc Disease
|
Anemia, Sickle Cell
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Hbsc Disease
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Sickle Cell-Hemoglobin C Disease Syndrome
|
Hb Ss Disease
|
Sickle Cell Trait
|
Drepanocytosis
|
Haemoglobin Sc Disease
|
Hb Sc Disease
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Hb-S/Hb-C Disease
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Hb-Ss Disease Without Crisis
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Hemoglobin S Disease Without Crisis
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Sickle Cell Anaemia
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Sickle-Cell/Hb-C Disease Without Crisis
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Sickle Cell - Hemoglobin C Disease
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Hbs Disease
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Hemoglobin S Disease
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Sickling Disorder Due To Hemoglobin S
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SKCA
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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]
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Sickle-Cell Trait Haemoglobin Disease
|
Haemoglobin Sickle Cell Trait Disorder
|
Heterozygous Sickle Cell Trait
|
Hbas - [Heterozygous Haemoglobin S]
|
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Hemoglobinopathy |
|
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Plasmodium Vivax Malaria |
Malaria, Vivax
|
Malaria By Plasmodium Vivax
|
Vivax Malaria
|
Malaria Vivax
|
|
|
Beta-Thalassemia Major |
Cooley'S Anemia
|
Cooley Anemia
|
Mediterranean Anemia
|
|
|
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
|
|
|
Parasitic Protozoa Infectious Disease |
Protozoan Infections
|
Mastigophora Infectious Disease
|
Sarcomastigophora Infectious Disease
|
|
|
Hemoglobin D Disease |
Hb-D Disease
|
Punjab Disease
|
Los Angeles Disease
|
Hb D Los Angeles Disease
|
Hb D Punjab Disease
|
|
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Glucosephosphate Dehydrogenase Deficiency |
G6pd Deficiency
|
Glucose-6-Phosphate Dehydrogenase Deficiency
|
Deficiency Of Glucose-6-Phosphate Dehydrogenase
|
Glucose 6 Phosphate Dehydrogenase Deficiency
|
Deficiency Of G-6pd
|
G6pdd
|
|
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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
|
|
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Deficiency Anemia |
Anemia
|
Deficiency Anemias
|
Anaemia
|
|
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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
|
|
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