| Diseases |
Alias |
|
| Thrombocytopenia With Beta-Thalassemia, X-Linked |
|
XLTT
|
Thrombocytopenia, Platelet Dysfunction, Hemolysis, And Imbalanced Globin Synthesis
|
|
Beta-Thalassemia-X-Linked Thrombocytopenia Syndrome
|
Gata1-Related X-Linked Cytopenia
|
|
X-Linked Thrombocytopenia With Beta-Thalassemia
|
Thrombocytopenia Platelet Dysfunction Hemolysis And Imbalanced Globin Synthesis
|
|
|
| Thrombocytopenia, X-Linked, With Or Without Dyserythropoietic Anemia |
|
XDAT
|
XLTDA
|
|
Thrombocytopenia With Congenital Dyserythropoietic Anemia
|
Congenital Dyserythropoietic Anemia With Thombocytopenia
|
|
X-Linked Congenital Dyserythropoietic Anemia With Thrombocytopenia
|
X-Linked Dyserythropoietic Anemia And Thrombocytopenia
|
|
Thrombocytopenia, X-Linked, With Dyserythropoietic Anemia
|
Thrombocytopenia, X-Linked, Without Dyserythropoietic Anemia
|
|
|
| Anemia, X-Linked, With Or Without Neutropenia And/Or Platelet Abnormalities |
|
X-Linked Dyserythropoietic Anemia
|
X-Linked Dyserythropoietic Anemia With Abnormal Platelets And Neutropenia
|
|
XLANP
|
Anemia, X-Linked, With/Without Neutropenia And/Or Platelet Abnormalities
|
|
X-Linked Anemia With/Without Neutropenia And/Or Platelet Abnormalities
|
Anemia Without Thrombocytopenia, X-Linked
|
|
XLAWT
|
Anemia X-Linked With Variable Neutropenia
|
|
|
| Adenosine Deaminase, Elevated, Hemolytic Anemia Due To |
|
HAEADA
|
Erythrocyte Ada, Elevated, Hemolytic Anemia Due To
|
|
Hemolytic Anemia Due To Elevated Adenosine Deaminase
|
|
|
| Myeloproliferative Syndrome, Transient |
|
Transient Abnormal Myelopoiesis
|
Transient Myeloproliferative Syndrome
|
|
Transient Myeloproliferative Disease
|
Mst
|
|
Tam
|
Leukemia, Transient, Of Down Syndrome
|
|
Tmd
|
Leukemia, Transient
|
|
Transient Leukemia
|
Transient Leukemia Of Down Syndrome
|
|
|
| Acute Megakaryoblastic Leukemia In Down Syndrome |
|
|
| Hemolytic Anemia Due To Erythrocyte Adenosine Deaminase Overproduction |
|
|
| Acute Megakaryocytic Leukemia |
|
Acute Megakaryoblastic Leukemia
|
Acute Megakaryoblastic Leukaemia
|
|
Megakaryocytic Myelosis
|
Thrombocytic Leukaemia
|
|
Amkl
|
Aml M7
|
|
Acute Myeloblastic Leukemia Type 7
|
Acute Myeloid Leukemia M7
|
|
Megakaryoblastic Leukemia Acute
|
Leukemia, Megakaryoblastic, Acute
|
|
Acute Myeloid Leukaemia, M7
|
Acute Megakaryocytic Leukaemia
|
|
Acute Megakaryoblastic Leukaemia, Fab M7
|
Fab M7
|
|
Malignant Megakaryocytosis
|
M7 - Acute Megakaryoblastic Leukaemia
|
|
Megakaryoblastic Leukaemia
|
Megakaryocytic Leukaemia
|
|
Acute Megakaryoblastic Leukaemia, Nos
|
Acute Megakaryoblastic Leukaemia Without Mention Of Remission
|
|
|
| Down Syndrome |
|
Trisomy 21
|
Complete Trisomy 21 Syndrome
|
|
Down'S Syndrome
|
Trisomy 21 Syndrome
|
|
Down'S Syndrome - Trisomy 21
|
Downs Syndrome
|
|
G Trisomy
|
47,Xx,+21
|
|
47,Xy,+21
|
Trisomy G
|
|
Down Syndrome, Susceptibility To
|
Chromosome 21 Trisomy
|
|
Trisomy 21 Nos
|
Abnormal Autosomes 21
|
|
|
| Acute Basophilic Leukemia |
|
|
| 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
|
|
|
| Porphyria, Congenital Erythropoietic |
|
Congenital Erythropoietic Porphyria
|
Gunther Disease
|
|
CEP
|
Uros Deficiency
|
|
Günther Disease
|
Uroporphyrinogen Iii Synthase Deficiency
|
|
Congenital Porphyria
|
Uroporphyrinogen Iii Synthase, Deficiency Of
|
|
Porphyria, Erythropoietic, Congenital
|
Porphyria, Erythropoietic
|
|
Deficiency Of Uroporphyrinogen Iii Synthase
|
|
|
| Diamond-Blackfan Anemia 1 |
|
Aase Syndrome
|
DBA1
|
|
Erythrogenesis Imperfecta
|
Aase-Smith Syndrome Ii
|
|
Dba
|
Blackfan-Diamond Syndrome
|
|
Bds
|
Anemia, Congenital Hypoplastic, Of Blackfan And Diamond
|
|
Anemia, Congenital Erythroid Hypoplastic
|
Red Cell Aplasia, Pure, Hereditary
|
|
Aregenerative Anemia, Chronic Congenital
|
Rps19-Related Diamond-Blackfan Anemia
|
|
Chronic Congenital Aregenerative Anemia
|
Congenital Erythroid Hypoplastic Anemia
|
|
Congenital Hypoplastic Anemia Of Blackfan And Diamond
|
Pure Hereditary Red Cell Aplasia
|
|
Anemia, Diamond-Blackfan, Type 1
|
Anemia, Diamond-Blackfan
|
|
Aase Smith Syndrome 2
|
Familial Hypoplastic Anaemia With Malformations
|
|
Constitutional Pure Red Cell Aplasia
|
|
|
| Dyserythropoietic Anemia And Thrombocytopenia |
|
Dyserythropoietic Anemia With Thrombocytopenia
|
Gata-1-Related Thrombocytopenia With Dyserythropoiesis
|
|
Gata1-Related Cytopenia
|
Gata1-Related X-Linked Cytopenia
|
|
X-Linked Macrothrombocytopenia
|
Macrothrombocytopenia, X-Linked
|
|
|
| Erythroleukemia |
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| 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
|
|
|
| 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
|
|
|
| Thalassemia Minor |
|
|
| Myeloid Leukemia Associated With Down Syndrome |
|
|
| Myelofibrosis |
|
Primary Myelofibrosis
|
Agnogenic Myeloid Metaplasia
|
|
Idiopathic Myelofibrosis
|
Myeloid Metaplasia
|
|
Myelofibrosis With Myeloid Metaplasia
|
Osteomyelofibrosis
|
|
Megakaryocytic Myelosclerosis
|
Myelosclerosis
|
|
Chronic Idiopathic Myelofibrosis
|
Myelofibrosis, Idiopathic
|
|
Myelofibrosis With Myeloid Metaplasia, Somatic
|
Myelofibrosis, Somatic
|
|
Aleukemic Myelosis
|
Bone Marrow Fibrosis
|
|
MYELOF
|
MMM
|
|
Agnogenic Myeloid Metaplasia With Myelofibrosis
|
Ammm
|
|
Myelosclerosis With Myeloid Metaplasia
|
Myelofibrosis Nos
|
|
|
| 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
|
|
|
| Gray Platelet Syndrome |
|
Platelet Alpha-Granule Deficiency
|
GPS
|
|
Bdplt4
|
Bleeding Disorder, Platelet-Type, 4
|
|
Grey Platelet Syndrome
|
Platelet-Type Bleeding Disorder 4
|
|
Marked Decrease Or Absence Of Alpha-Granules And Of Platelet-Specific Alpha-Granule Proteins
|
Deficient Alpha Granule Syndrome
|
|
Platelet Alpha Granule Deficiency
|
Platelet Granule Defect
|
|
Alpha Storage Pool Deficiency
|
Bleeding Disorder Platelet-Type 4
|
|
|
| Neonatal Leukemia |
|
|
| Thrombocytopenia 1 |
|
Xlt
|
THC1
|
|
Thrombocytopenia, X-Linked
|
Thrombocytopenia, X-Linked, Intermittent
|
|
X-Linked Thrombocytopenia
|
X-Linked Thrombocytopenia With Normal Platelets
|
|
Thc
|
Thrombocytopenia, X-Linked, 1
|
|
Thrombocytopenia X-Linked
|
Thrombocytopenia X-Linked 1
|
|
|
| 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, 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
|
|
|
| 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
|
|
|
| Myeloproliferative Neoplasm |
|
Myeloproliferative Disorder
|
Chronic Myeloproliferative Disease
|
|
Myeloproliferative Neoplasms
|
Chronic Myeloproliferative Disorder
|
|
Cmpd
|
Cmpd, U
|
|
Chronic Myeloproliferative Disorders
|
Mpd
|
|
Mpn
|
Myeloproliferative Disorders
|
|
Myeloproliferative Disease
|
Campomelic Dysplasia
|
|
|
| Acute Leukemia |
|
Stem Cell Leukaemia
|
Stem Cell Leukemia
|
|
Acute Leukemias
|
Acute Undifferentiated Leukemia
|
|
Undifferentiated Leukemia
|
Acute Leukaemia Of Unspecified Cell Type Without Mention Of Remission
|
|
Blast Cell Leukaemia
|
Blast Leukaemia
|
|
Blastic Leukaemia
|
Undifferentiated Leukaemia
|
|
|
| Essential Thrombocythemia |
|
Essential Thrombocytosis
|
Familial Thrombocytosis
|
|
Hemorrhagic Thrombocythemia
|
Hereditary Thrombocythemia
|
|
Primary Thrombocytosis
|
Idiopathic Thrombocythemia
|
|
Primary Thrombocythemia
|
Thrombocythemia, Essential
|
|
Essential Thrombocythaemia
|
Et
|
|
Familial Thrombocythemia
|
Thrombocythemia Essential
|
|
|
| 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
|
|
|
| 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
|
|
|
| Cutaneous Porphyria |
|
Porphyria, Erythropoietic
|
Erythropoietic Porphyria
|
|
|
| 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
|
|
|
| Myelodysplastic Syndrome |
|
Myelodysplastic Syndromes
|
Myelodysplasia
|
|
MDS
|
Myelodysplastic Syndrome Included
|
|
Myelodysplastic Syndrome, Susceptibility To, Included
|
Myelodysplastic Syndrome, Somatic
|
|
Myelodysplastic Syndrome, Susceptibility To
|
|
|
| Childhood Acute Megakaryoblastic Leukemia |
|
Pediatric Non-Down Syndrome Acute Megakaryoblastic Leukemia
|
|
|
| Alzheimer Disease 19 |
|
AD19
|
Alzheimer'S Disease 19
|
|
Alzheimer Disease 19, Late-Onset
|
Alzheimer Disease 19 Late Onset
|
|
Late-Onset Alzheimer Disease
|
Alzheimer Disease, Late Onset, Susceptibility To, Type 19
|
|
Alzheimer Disease, Late Onset
|
|
|
| Polycythemia |
|
Erythrocythemia
|
Polycythemia Vera
|
|
Polycythaemia Due To High Altitude
|
|
|
| Chromosomal Duplication Syndrome |
|
|
| 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
|
|
|
| Pseudo-Von Willebrand Disease |
|
Bdplt3
|
Von Willebrand Disease, Platelet-Type
|
|
VWDP
|
Platelet-Type Bleeding Disorder 3
|
|
Platelet Type-Von Willebrand Disease
|
Pt-Vwd
|
|
Von Willebrand Disease Platelet-Type
|
Von Willebrand Disease, Platelet Type
|
|
Pseudo Von Willebrand Disease
|
Bleeding Disorder, Platelet-Type, 3
|
|
Pseudo-Von Willebrand Disease Type 2b
|
Bleeding Disorder Platelet-Type 3
|
|
Pseudo-Vwd
|
|
|
| Immunodeficiency 21 |
|
Monocytopenia And Mycobacterial Infection Syndrome
|
Monomac
|
|
Gata2 Deficiency
|
Monocytopenia With Susceptibility To Infections
|
|
Dcml
|
IMD21
|
|
Dendritic Cell, Monocyte, B Lymphocyte, And Natural Killer Lymphocyte Deficiency
|
Monocytopenia With Susceptibility To Mycobacterial, Fungal, And Papillomavirus Infections And Myelodysplasia
|
|
Combined Immunodeficiency With Susceptibility To Mycobacterial, Viral, And Fungal Infections
|
Combined Immunodeficiency With Susceptibility To Mycobacterial, Viral And Fungal Infections
|
|
Dendritic Cell, Monocyte, B And Nk Lymphoid Deficiency
|
Monocyte-B-Natural Killer-Dendritic Cell Deficiency Syndrome
|
|
Monocytopenia With Mycobacterial, Fungal, And Papillomavirus Infections And Myelodysplasia
|
Combined Immunodeficiency With Mycobacterial, Viral, And Fungal Infections
|
|
Monocyte - B - Natural Killer - Dendritic Cell Deficiency
|
Combined Immunodeficiency With Susceptibility To Mycobacterial Viral And Fungal Infections
|
|
Dendritic Cell Monocyte Lymphocyte B And Natural Killer Lymphocyte Deficiency
|
Monocytopenia With Susceptibility To Mycobacterial Fungal And Papillomavirus Infections And Myelodysplasia
|
|
|
| Amegakaryocytic Thrombocytopenia, Congenital |
|
Congenital Amegakaryocytic Thrombocytopenia
|
CAMT
|
|
Thrombocytopenia, Congenital Amegakaryocytic
|
Congenital Amegakaryocytic Thrombocytopenic Purpura
|
|
Thrombocytopenia Congenital Amegakaryocytic
|
Thrombocytopenia, Amegakaryocytic, Congenital
|
|
|
| Plasmodium Vivax Malaria |
|
Malaria, Vivax
|
Malaria By Plasmodium Vivax
|
|
Vivax Malaria
|
Malaria Vivax
|
|
|
| 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
|
|
|
| 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]
|
|
|
| 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
|
|
|
| Diamond-Blackfan Anemia 11 |
|
DBA11
|
Rpl26-Related Diamond-Blackfan Anemia
|
|
Anemia, Diamond-Blackfan, Type 11
|
|
|
| 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
|
|
|
| Alpha-Thalassemia Myelodysplasia Syndrome |
|
ATMDS
|
Acquired Hemoglobin H Disease
|
|
Alpha-Thalassemia Myelodysplasia Syndrome, Somatic
|
Acquired Hbh Disease
|
|
Alpha-Thalassemia-Myelodysplastic Syndrome
|
Hemoglobin H Disease, Acquired
|
|
Acquired Alpha-Thalassemia With Myelodysplastic Syndrome
|
Hemoglobin H Disease Acquired
|
|
Thalassemia, Alpha, Myelodysplasia Syndrome, Somatic
|
|
|
| Leukemia, Chronic Myeloid |
|
Chronic Myeloid Leukemia
|
Chronic Myelogenous Leukemia
|
|
CML
|
Chronic Granulocytic Leukemia
|
|
Leukemia, Philadelphia Chromosome-Positive, Resistant To Imatinib
|
Chronic Myeloid Leukaemia
|
|
Chronic Granulocytic Leukaemia
|
Chronic Myelogenous Leukaemia
|
|
Myeloid Leukemia, Chronic
|
Leukemia, Chronic Myelogenous
|
|
Leukemia, Chronic Myeloid, Philadelphia Chromosome Positive, Somatic
|
Cml - Chronic Myelogenous Leukemia
|
|
Cgl
|
Chronic Myelocytic Leukemia
|
|
Leukemia, Chronic Myeloid, Atypical
|
ACML
|
|
Atypical Chronic Myeloid Leukemia Bcr-Abl1 Negative
|
Myeloid Leukemia Chronic
|
|
Leukemia, Myeloid, Chronic
|
Leukemia, Myeloid, Chronic, Atypical, Bcr-Abl Negative
|
|
Cml- [Chronic Myeloid Leukaemia]
|
Cgl - [Chronic Granulocytic Leukaemia]
|
|
Chronic Myelocytic Leukaemia
|
|
|
| Hemoglobinopathy |
|
|
| Congenital Hemolytic Anemia |
|
Anemia Hemolytic Congenital
|
Anemia, Hemolytic, Congenital
|
|
Congenital Hemolytic Anaemia
|
Hereditary Hemolytic Anaemia
|
|
Hereditary Hemolytic Anemia
|
|
|
| Chromosomal Disease |
|
Chromosomal Disorders
|
Congenital Chromosomal Disease
|
|
|
| Beta-Thalassemia Major |
|
Cooley'S Anemia
|
Cooley Anemia
|
|
Mediterranean Anemia
|
|
|
| Leukemia, Acute Lymphoblastic |
|
Acute Lymphoblastic Leukemia
|
ALL
|
|
Acute Lymphocytic Leukemia
|
Leukemia, Acute Lymphocytic, Susceptibility To, 1
|
|
Acute Lymphoblastic Leukaemia
|
Precursor Lymphoblastic Lymphoma/Leukemia
|
|
Precursor Lymphoid Neoplasm
|
Leukemia, Acute Lymphoblastic, Susceptibility To
|
|
B-Cell Acute Lymphoblastic Leukemia
|
Leukemia, Acute Lymphocytic 1
|
|
Acute Lymphocytic Leukaemia
|
Acute Lymphoblastic Leukemia/Lymphoma
|
|
All1
|
Childhood Acute Lymphoblastic Leukemia
|
|
Leukemia Acute Lymphoblastic 1
|
Leukemia Acute Lymphoblastic B-Hyperdiploid
|
|
Leukemia Acute Lymphocytic
|
Leukemia Acute Lymphocytic 1
|
|
Leukemia B-Cell Acute Lymphoblastic
|
Leukemia T-Cell Acute Lymphoblastic
|
|
Leukemia, Acute Lymphoblastic, 3
|
ALL3
|
|
Lymphoblastic Leukemia Acute
|
Leukemia, Acute, Lymphoblastic
|
|
Precursor Cell Lymphoblastic Leukemia Lymphoma
|
Leukemia, Lymphocytic, Acute, L1
|
|
Leukemia, Acute Lymphoblastic, Susceptibility To, 3
|
|
|
| Acute Promyelocytic Leukemia |
|
Leukemia, Acute Promyelocytic
|
Acute Myeloblastic Leukemia Type 3
|
|
Aml M3
|
APL
|
|
Leukemia, Acute Promyelocytic, Somatic
|
Aml With T(15
|
|
17)(Q22
|
Q12)
|
|
(Pml/Raralpha) And Variants
|
Apml
|
|
Acute Myeloblastic Leukemia 3
|
Acute Myeloid Leukemia With T(15
|
|
17)(Q22
|
Q12)
|
|
(Pml/Raralpha) And Variants
|
Acute Myeloblastic Leukaemia Type 3
|
|
Acute Myeloid Leukaemia M3
|
Acute Myeloid Leukemia M3
|
|
Acute Promyelocytic Leukaemia
|
M3 Anll
|
|
Myeloid Leukemia, Acute, M3
|
Leukemia Promyelocytic Acute
|
|
Leukemia, Promyelocytic, Acute
|
Leukemia, Acute, Promyelocytic
|
|
|
| Childhood Leukemia |
|
|
| 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]
|
|
|
| Bernard-Soulier Syndrome |
|
Giant Platelet Syndrome
|
BSS
|
|
Von Willebrand Factor Receptor Deficiency
|
Bdplt1
|
|
Platelet Glycoprotein Ib Deficiency
|
Bernard-Soulier Syndrome, Type A1
|
|
Bernard-Soulier Syndrome, Type B
|
Bernard Soulier Syndrome
|
|
Deficiency Of Platelet Glycoprotein 1b
|
Hemorrhagiparous Thrombocytic Dystrophy
|
|
Bernard-Soulier Syndrome Type C
|
Bleeding Disorder, Platelet-Type, 1
|
|
Glycoprotein Ib, Platelet, Deficiency Of
|
Giant Platelet Disorder, Isolated
|
|
Giant Platelet Disease
|
Macrothrombocytopenia, Familial Bernard-Soulier Type
|
|
Bernard-Soulier Syndrome, Type C
|
Bernard - Soulier Thrombopathy
|
|
Hemorrhagic Dystrophic Thrombocytopenia
|
Thrombopathy, Bernard-Soulier
|
|
Platelet Glycoprotein 1b, Deficiency Of
|
Hemorrhagioparous Thrombocytic Dystrophy
|
|
Bernard-Soulier Syndrome Type A1
|
Bernard-Soulier Syndrome Type B
|
|
Bleeding Disorder Platelet-Type 1
|
Gpd
|
|
Macrothrombocytopenia, Familial, Bernard-Soulier Type
|
|
|
| Blood Platelet Disease |
|
Platelet Disorder
|
Blood Platelet Disorders
|
|
Thrombocytopathy
|
Platelet Dysfunction
|
|
Platelet Disorders
|
Qualitative Platelet Deficiency
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Shwachman-Diamond Syndrome 1 |
|
Shwachman-Diamond Syndrome
|
Shwachman Syndrome
|
|
Shwachman-Bodian-Diamond Syndrome
|
Sds
|
|
Pancreatic Insufficiency And Bone Marrow Dysfunction
|
Shwachman-Bodian Syndrome
|
|
SDS1
|
Lipomatosis Of Pancreas, Congenital
|
|
Congenital Lipomatosis Of Pancreas
|
Shwachman-Diamond Type Metaphyseal Dysplasia
|
|
Metaphyseal Chondrodysplasia, Shwachman Type
|
Shwachman-Diamond-Oski 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
|
|
|
| Dyskeratosis Congenita |
|
Dyskeratosis Congenita Autosomal Dominant
|
Dc
|
|
Dkc
|
Zinsser-Engman-Cole Syndrome
|
|
Dyskeratosis Congenita, Autosomal Dominant
|
Autosomal Dominant Dyskeratosis Congenita
|
|
Dkca
|
Dyskeratosis Congenita Scoggins Type
|
|
Zinsser-Cole-Engman Syndrome
|
X-Linked Dyskeratosis Congenita
|
|
Hoyeraal-Hreidarsson Syndrome
|
|
|
