| 疾病名称 |
别名 |
|
| Anemia, Congenital Dyserythropoietic, Type Iv |
|
CDAN4
|
Congenital Dyserythropoietic Anemia Type Iv
|
|
Congenital Dyserythropoietic Anemia Type 4
|
Cda Iv
|
|
Cda Due To Klf1 Mutation
|
Cda Type 4
|
|
Cda Type Iv
|
Congenital Dyserythropoietic Anemia Due To Klf1 Mutation
|
|
Cda, Type Iv
|
Dyserythropoietic Anemia, Congenital, Type Iv
|
|
Congenital Dyserythropoietic Anaemia Due To Klf1 Mutation
|
Congenital Dyserythropoietic Anaemia Type 4
|
|
Congenital Dyserythropoietic Anaemia Type Iv
|
Anemia, Congenital Dyserythropoietic, 4
|
|
Anemia, Dyserythropoietic Congenital, Type Iv
|
Anemia, Dyserythropoietic, Congenital, Type Iv
|
|
|
| Fetal Hemoglobin Quantitative Trait Locus 6 |
|
HBFQTL6
|
Hereditary Persistence Of Fetal Hemoglobin, Klf1-Related
|
|
Hereditary Persistence Of Fetal Hemoglobin
|
Hemoglobin, Fetal, Quantitative Trait Locus 6
|
|
|
| Hereditary Persistence Of Fetal Hemoglobin-Beta-Thalassemia Syndrome |
|
Hpfh-Beta-Thalassemia Syndrome
|
|
|
| Hereditary Persistence Of Fetal Hemoglobin-Sickle Cell Disease Syndrome |
|
Hpfh-Sickle Cell Disease Syndrome
|
|
|
| Hemoglobinopathy |
|
|
| Erythroleukemia |
|
|
| 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
|
|
|
| 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
|
|
|
| Neonatal Anemia |
|
Anemia Neonatal
|
Anemia, Neonatal
|
|
Anaemia Neonatal
|
Neonatal Anaemia
|
|
|
| Alpha-Thalassemia |
|
Alpha Thalassemia
|
Alpha Thalassaemia
|
|
Alpha Plus Thalassemia
|
Thalassemia, Alpha-
|
|
Thalassemias, Alpha-
|
A-Thalassemia
|
|
Α-Thalassemia
|
A-THAL
|
|
Thalassemia
|
Alpha Thalassaemia Syndrome
|
|
|
| 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
|
|
|
| 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
|
|
|
| Anemia, Congenital Dyserythropoietic, Type Iiia |
|
Congenital Dyserythropoietic Anemia, Type Iii
|
Cdan3
|
|
Congenital Dyserythropoietic Anemia Type Iii
|
Cda Iii
|
|
Congenital Dyserythropoietic Anemia Type 3
|
CDAN3A
|
|
Dyserythropoietic Anemia, Congenital, Type Iiia
|
Cda, Type Iiia
|
|
Anemia, Congenital Dyserythropoietic, Type Iii
|
Anemia With Multinucleated Erythroblasts
|
|
Cda Type 3
|
Cda Type Iii
|
|
Dyserythropoietic Anemia, Congenital Type 3
|
Cda, Type Iii
|
|
Erythroreticulosis, Hereditary Benign
|
Anaemia With Multinucleated Erythroblasts
|
|
Congenital Dyserythropoietic Anaemia Type 3
|
Congenital Dyserythropoietic Anaemia Type Iii
|
|
Hereditary Benign Erythroreticulosis
|
Anemia, Congenital Dyserythropoietic, 3a
|
|
Anemia With Multinucleated Erythroblasts Erythroreticulosis, Hereditary Benign
|
|
|
| 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 |
|
|
| 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
|
|
|
| Congenital Hemolytic Anemia |
|
Anemia Hemolytic Congenital
|
Anemia, Hemolytic, Congenital
|
|
Congenital Hemolytic Anaemia
|
Hereditary Hemolytic Anaemia
|
|
Hereditary Hemolytic Anemia
|
|
|
| Anemia, Congenital Dyserythropoietic, Type Ii |
|
Congenital Dyserythropoietic Anemia Type Ii
|
CDAN2
|
|
Cda Ii
|
Hereditary Erythroblastic Multinuclearity With Positive Acidified-Serum Test
|
|
Cda Type Ii
|
Congenital Dyserythropoietic Anemia Type 2
|
|
Hereditary Erythroblastic Multinuclearity With A Positive Acidified-Serum Test
|
Sec23b-Cdg
|
|
Congenital Dyserythropoietic Anemia, Type Ii
|
Dyserythropoietic Anemia, Hempas Type
|
|
Hempas
|
Cda Type 2
|
|
Dyserythropoietic Anemia, Congenital, Type Ii
|
Cda, Type Ii
|
|
Congenital Dyserythropoietic Anaemia Type 2
|
Congenital Dyserythropoietic Anaemia Type Ii
|
|
Anemia, Dyserythropoietic, Congenital Type 2
|
Hempas Anemia
|
|
Dyserythropoietic Anemia, Congenital Type 2
|
Anemia, Congenital Dyserythropoietic, 2
|
|
Dyserythropoietic Anemia Hempas Type
|
Anemia, Dyserythropoietic Congenital, Type Ii
|
|
Anemia, Dyserythropoietic, Congenital, Type Ii
|
|
|
| Hemoglobin E Disease |
|
Hemoglobin E
|
Hb-E Disease
|
|
|
| Fetal Hemoglobin Quantitative Trait Locus 1 |
|
Hereditary Persistence Of Fetal Hemoglobin
|
Delta-Beta-Thalassemia
|
|
Delta-Beta Thalassemia
|
Delta Beta-Thalassemia
|
|
HBFQTL1
|
Hemoglobin F, Hereditary Persistence Of
|
|
Hpfh
|
Hereditary Persistence Of Fetal Hemoglobin, Hb Gene Cluster-Related
|
|
Hemoglobin, Fetal, Quantitative Trait Locus 1
|
Hereditary Persistence Of Fetal Hemoglobin Thalassemia
|
|
Hpfh - [Hereditary Persistence Of Fetal Haemoglobin]
|
Fetal Haemoglobin
|
|
Persistence Of Fetal Haemoglobin
|
Persistent Haemoglobin F
|
|
|
| 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
|
|
|
| Beta-Thalassemia Major |
|
Cooley'S Anemia
|
Cooley Anemia
|
|
Mediterranean Anemia
|
|
|
| Congenital Nonspherocytic Hemolytic Anemia |
|
Hereditary Non-Spherocytic Hemolytic Anemia
|
Hereditary Nonspherocytic Hemolytic Anemia
|
|
Anemia, Hemolytic, Congenital Nonspherocytic
|
Congenital Nonspherocytic Hemolytic Anaemia
|
|
Hereditary Nonspherocytic Hemolytic Anaemia
|
Hnsha
|
|
|
| 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]
|
|
|
| Autosomal Dominant Beta Thalassemia |
|
Inclusion Body Beta-Thalassemia
|
|
|
| Cutaneous Porphyria |
|
Porphyria, Erythropoietic
|
Erythropoietic Porphyria
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Hemoglobin C Disease |
|
Hb C Disease
|
Hemoglobin C
|
|
Hb-C Disease
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| 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
|
|
|
| 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
|
|
|
