| Diseases |
Alias |
|
| Diamond-Blackfan Anemia-Like |
|
|
| Erythrocytosis, Familial, 5 |
|
ECYT5
|
Familial Erythrocytosis 5
|
|
|
| Microvascular Complications Of Diabetes 2 |
|
Microvascular Complications Of Diabetes, Susceptibility To, 2
|
MVCD2
|
|
Diabetic Nephropathy
|
Proliferative Diabetic Retinopathy
|
|
Proliferative Retinopathy, Diabetic
|
Proliferative Retinopathy, Diabetic, Susceptibility To
|
|
End-Stage Renal Disease, Diabetic
|
End-Stage Renal Disease, Diabetic, Susceptibility To
|
|
Diabetic End-Stage Renal Disease
|
|
|
| Autosomal Dominant Secondary Polycythemia |
|
Autosomal Dominant Secondary Erythrocytosis
|
|
|
| Uremia |
|
|
| End Stage Renal Disease |
|
End Stage Renal Failure
|
End-Stage Kidney Disease
|
|
Kidney Failure, Chronic
|
Chronic Kidney Disease Stage 5
|
|
|
| Pure Red-Cell Aplasia |
|
Pure Red Cell Aplasia
|
Primary Red Cell Aplasia
|
|
Red Cell Hypoplasia
|
Prca
|
|
Red-Cell Aplasia Pure
|
Red-Cell Aplasia, Pure
|
|
|
| Acquired Polycythemia |
|
Secondary Polycythemia
|
Polycythemia, Secondary
|
|
Secondary Erythrocytosis
|
Polycythemia Secondary
|
|
|
| Ocular Hypertension |
|
Hypertension, Ocular
|
Intraocular Pressure Increase
|
|
Oh - [Ocular Hypertension]
|
Oht - [Ocular Hypertension]
|
|
|
| Neonatal Anemia |
|
Anemia Neonatal
|
Anemia, Neonatal
|
|
Anaemia Neonatal
|
Neonatal Anaemia
|
|
|
| Iron Deficiency Anemia |
|
Iron-Deficiency Anemia
|
Fe Deficiency Anaemia
|
|
Ida - [Iron Deficiency Anemia]
|
Fe - [Iron] Deficiency Anemia Nos
|
|
|
| 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
|
|
|
| Polycythemia |
|
Erythrocythemia
|
Polycythemia Vera
|
|
Polycythaemia Due To High Altitude
|
|
|
| Thrombocytosis |
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Hemangioblastoma |
|
Capillary Hemangioblastoma
|
|
|
| Hypertensive Encephalopathy |
|
Encephalopathy, Hypertensive
|
|
|
| Primary Polycythemia |
|
Familial Erythrocytosis
|
Familiar Polycythemia
|
|
Benign Familial Polycythemia
|
Congenital Erythrocytosis
|
|
Familial Polycythemia
|
Hereditary Erythrocytosis
|
|
Primary Familial Polycythemia
|
Erythrocytosis, Familial
|
|
Polycythemia Vera
|
Primary Familial Polycythaemia
|
|
Primary Inherited Polycythaemia
|
|
|
| Refractory Anemia |
|
Anemia Refractory
|
Refractory Anemias
|
|
Refractory Anemia, Without Ringed Sideroblasts, Without Excess Blasts
|
Refractory Anaemia Without Sideroblasts
|
|
Refractory Anaemia With Sideroblasts
|
Acquired Idiopathic Sideroblastic Anaemia
|
|
Primary Acquired Sideroblastic Anaemia
|
Refractory Sideroblastic Anaemia
|
|
Refractory Anaemia With Excess Blasts
|
Raeb - [Refractory Anaemia With Excess Blasts] Nos
|
|
Raeb - [Refractory Anaemia With Excess Blasts]
|
Rars-T [Refractory Anaemia With Ringed Sideroblasts Associated With Marked Thrombocytosis]
|
|
|
| Rh Isoimmunization |
|
Rh Incompatibility Affecting Management Of Mother
|
|
|
| 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
|
|
|
| Chronic Kidney Disease |
|
Chronic Renal Disease
|
Chronic Kidney Failure
|
|
Ckd
|
Chronic Renal Failure
|
|
Kidney Failure, Chronic
|
Chronic Renal Failure Syndrome
|
|
Crf
|
Renal Failure - Chronic
|
|
Renal Failure Chronic
|
Chronic Kidney Diseases
|
|
Chronic Kidney Disease Stage 5
|
Ckd - [Chronic Kidney Disease]
|
|
Crf - [Chronic Renal Failure]
|
Chronic Kidney Impairment
|
|
Chronic Renal Impairment
|
Chronic Kidney Shutdown
|
|
Chronic Hypoxic Kidney Failure
|
Chronic Kidney Collapse
|
|
Chronic Renal Insufficiency
|
Chronic Kidney Toxaemia
|
|
Chronic Kidney Hypofunction
|
Chronic Renal Suppression
|
|
Chronic Renal Failure, Stage 5
|
Ckd - [Chronic Kidney Disease] Stage 5
|
|
End Stage Kidney Failure
|
End Stage Renal Failure
|
|
End Stage Kidney Disease
|
End Stage Renal Disease
|
|
End Stage Chronic Renal Failure
|
Esrf - [End Stage Renal Failure]
|
|
Esrd - [End Stage Renal Diseases]
|
Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
|
|
|
| Kidney Disease |
|
Renal Failure
|
Kidney Failure
|
|
Kidney Diseases
|
Nephropathy
|
|
Abnormality Of The Kidney
|
Impaired Renal Function Disease
|
|
Renal Anomaly
|
Kidney Dysfunction
|
|
Renal Disease
|
Nephropathies
|
|
Renal Failure Adverse Event
|
Abnormal Renal Function
|
|
|
| Erythroleukemia |
|
|
| Ischemia |
|
|
| Acute Radiation Syndrome |
|
|
| Anemia Of Prematurity |
|
|
| Iritis |
|
|
| Diabetic Neuropathy |
|
|
| Iron Metabolism Disease |
|
Iron Deficiency
|
Iron Disorder
|
|
Iron Metabolism Disorders
|
Disorder Of Iron Metabolism
|
|
Iron
|
Fe Deficiency
|
|
Iron Storage Disease
|
Iron Storage Disorder
|
|
|
| Secondary Hyperparathyroidism |
|
Hyperparathyroidism Secondary
|
Hyperparathyroidism, Secondary
|
|
Secondary Hyperparathyroidism Nec
|
|
|
| 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
|
|
|
| Hypersplenism |
|
Hypersplenia
|
Big Spleen Syndrome
|
|
Hyperfunction Of Spleen
|
Increased Splenic Activity
|
|
Spleen Metaplasia
|
Splenic Metaplasia
|
|
|
| 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
|
|
|
| Calciphylaxis |
|
|
| 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
|
|
|
| Chromosome 5q Deletion Syndrome |
|
5q- Syndrome
|
Mar
|
|
Myelodysplastic Syndrome Associated With Isolated Del Chromosome Abnormality
|
Macrocytic Anemia, Refractory, Due To 5q Deletion, Somatic
|
|
5q Deletion Syndrome
|
5q Minus Syndrome
|
|
Refractory Macrocytic Anemia Due To 5q Deletion
|
Myelodysplastic Syndrome With Isolated Del
|
|
Macrocytic Anemia, Refractory, Due To 5q Deletion
|
5q- Syndrome, Refractory Macrocytic Anemia Due To 5q Deletion
|
|
5q Syndrome
|
Chromosome 5q Deletion
|
|
Myelodysplastic Syndrome With 5q Deletion
|
Myelodysplastic Syndrome With 5q Deletion Syndrome
|
|
Anemia, Macrocytic, Refractory, Due To 5q Deletion, Somatic
|
5q-Syndrome
|
|
Chromosome 5, Trisomy 5q
|
Loss Of Chromosome 5q
|
|
5 Q- Syndrome
|
|
|
| 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
|
|
|
| Hyperparathyroidism |
|
Hyperparathyroidism And Other Disorders Of Parathyroid Gland
|
Parathyroid Hyperfunction
|
|
Hpth - [Hyperparathyroidism]
|
Parathyroid Gland Hyperfunction
|
|
Parathyroid Glandular Hyperfunction
|
|
|
| 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
|
|
|
| Pancytopenia |
|
|
| 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]
|
|
|
| Autonomic Neuropathy |
|
Diabetic Autonomic Neuropathy
|
|
|
| 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]
|
|
|
| Mirage Syndrome |
|
Myelodysplasia, Infection, Restriction Of Growth, Adrenal Hypoplasia, Genital Phenotypes, And Enteropathy
|
MIRAGE
|
|
Myelodysplasia, Infection, Restriction Of Growth, Adrenal Hypoplasia, Genital Phenotypes, Enteropathy
|
Myelodysplasia-Infection-Restriction Of Growth-Adrenal Hypoplasia-Genital Anomalies-Enteropathy Syndrome
|
|
Myelodysplasia-Infection-Restriction Of Growth-Adrenal Hypoplasia-Genital Phenotypes-Enteropathy Syndrome
|
Bone Marrow Diseases
|
|
|
| Congestive Heart Failure |
|
Congestive Heart Disease
|
Heart Failure
|
|
Cardiac Failure Congestive
|
Chf
|
|
Weak Heart
|
Heart Failure Congestive
|
|
Ccf - [Congestive Cardiac Failure]
|
Chf - [Congestive Heart Failure]
|
|
Congestive Cardiac Diseases
|
Congested Heart Failure
|
|
Congestive Cardiac Failure
|
Cardiac Anasarca
|
|
Cardiac Oedema
|
Cardiac Stasis
|
|
Cardiovascular Oedema
|
Cardiac Hydrops
|
|
Congestive Failure
|
Heart Congestion
|
|
Heart Fluid
|
Oedematous Heart
|
|
|
| Ureteral Obstruction |
|
|
| Nutritional Deficiency Disease |
|
Malnutrition
|
Nutritional Disorder
|
|
Nutritional Deficiency
|
Nutrition
|
|
Deficiency Diseases
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
|
Nutrition Disorders
|
|
|
| Hemosiderosis |
|
Haemosiderosis
|
Iron Overload
|
|
|
| Poems Syndrome |
|
Crow-Fukase Syndrome
|
Osteosclerotic Myeloma
|
|
Polyneuropathy Organomegaly
|
Polyneuropathy, Organomegaly, Endocrinopathy, M Protein, And Skin Changes Syndrome
|
|
Pep Syndrome
|
Polyneuropathy-Endocrinopathy-Plasma Cell Dyscrasia Syndrome
|
|
Takatsuki Syndrome
|
|
|
| Neutropenia |
|
|
| 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
|
|
|
| Myelodysplastic Syndrome |
|
Myelodysplastic Syndromes
|
Myelodysplasia
|
|
MDS
|
Myelodysplastic Syndrome Included
|
|
Myelodysplastic Syndrome, Susceptibility To, Included
|
Myelodysplastic Syndrome, Somatic
|
|
Myelodysplastic Syndrome, Susceptibility To
|
|
|
| Sickle Cell Disease |
|
Hbs Disease
|
Hemoglobin S Disease
|
|
Scd
|
Sickle Cell Disorders
|
|
Sickling Disorder Due To Hemoglobin S
|
Anemia, Sickle Cell
|
|
Hb-Ss Disease Without Crisis
|
Hbss Without Crisis
|
|
Sickle-Cell Anaemia Without Crisis
|
Scd - [Sickle Cell Disease]
|
|
Sca - [Sickle Cell Anaemia]
|
Sickle Cell Disease Nos
|
|
Sickle Cell Disorder
|
Sickle Cell Syndrome
|
|
Sickle-Cell Anaemia Nos
|
Sickle-Cell Disorder Nos
|
|
Haemoglobin S Disease
|
Haemoglobin Ss Disease
|
|
Hb S Disease
|
Hb Ss Disease
|
|
Herrick Anaemia
|
Hereditary Haemoglobinopathy Disorder Homozygous For Haemoglobin S
|
|
Sickle-Cell Haemoglobin Disease
|
Sickling Disorder Due To Haemoglobin S
|
|
Hb-Ss Disease With Crisis
|
Sickle Cell Crisis
|
|
Sickle-Cell Disorder With Crisis
|
Sickle-Cell Anaemia With Crisis
|
|
Hbss With Crisis
|
Hb S Disease With Mention Of Crisis
|
|
Haemoglobin Ss Disease With Crisis
|
Hb-Ss Disease With Vaso-Occlusive Pain
|
|
Vaso-Occlusive Crisis
|
|
|
| Microcytic Anemia |
|
Iron-Refractory Iron Deficiency Anemia
|
|
|
| Hemoglobinopathy |
|
|
| Stress Polycythemia |
|
Gaisbock'S Syndrome
|
Polycythemia, Emotional
|
|
Pseudopolycythaemia
|
Gaisboeck'S Syndrome
|
|
Pseudopolycythemia
|
Gaisbock Syndrome
|
|
Stress Erythrocytosis
|
Pseudo-Polycythemia
|
|
Relative Erythrocytosis
|
|
|
| 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
|
|
|
| Ovarian Clear Cell Cystadenocarcinoma |
|
|
| Fallopian Tube Mucinous Adenocarcinoma |
|
|
| Mixed Epithelial Tumor Of Ovary |
|
Ovarian Mixed Epithelial Tumor
|
Mixed Epithelial Tumour Of Ovary
|
|
Ovarian Mixed Epithelial Tumour
|
|
|
| Ovarian Clear Cell Malignant Adenofibroma |
|
Ovarian Clear Cell Adenocarcinofibroma
|
|
|
| Fallopian Tube Transitional Cell Carcinoma |
|
|
| Splenomegaly |
|
|
| 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
|
|
|
| Transient Erythroblastopenia Of Childhood |
|
Erythroblastopenia, Transient
|
Transient Acquired Pure Red Cell Aplasia
|
|
TEC
|
Familial Transient Erythroblastopenia Of Childhood
|
|
|
| Hemoglobinuria |
|
|
| Sleep Apnea |
|
|
| 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
|
|
|
| Thrombosis |
|
Thrombosis Of Blood Vessel
|
|
|
| Polycystic Kidney Disease |
|
Polycystic Kidney Diseases
|
Pkd
|
|
Polycystic Renal Disease
|
Kidney Disease, Polycystic
|
|
Polycystic Kidney, Autosomal Dominant
|
|
|
| Alpha-Thalassemia |
|
Alpha Thalassemia
|
Alpha Thalassaemia
|
|
Alpha Plus Thalassemia
|
Thalassemia, Alpha-
|
|
Thalassemias, Alpha-
|
A-Thalassemia
|
|
Α-Thalassemia
|
A-THAL
|
|
Thalassemia
|
Alpha Thalassaemia Syndrome
|
|
|
| Asphyxia Neonatorum |
|
Birth Asphyxia
|
Postnatal Asphyxia
|
|
Asphyxia - Birth
|
Asphyxia, In Liveborn Infant
|
|
Hypoxia Neonatorum
|
Hypoxia, In Liveborn Infant
|
|
Intrapartum Asphyxia
|
Neonatal Asphyxia
|
|
Newborn Asphyxia
|
Asphyxia In Liveborn Infant
|
|
Asphyxia Of Newborn Nos
|
Perinatal Asphyxia
|
|
Perinatal Hypoxia
|
Newborn Asphyxiation
|
|
|
| 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
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| Erythrocytosis, Familial, 1 |
|
ECYT1
|
Pfcp
|
|
Primary Familial And Congenital Polycythemia
|
Familial Erythrocytosis 1
|
|
Familial Erythrocytosis
|
Polycythemia, Primary Familial And Congenital
|
|
Autosomal Dominant Benign Erythrocytosis
|
Familial Erythrocytosis Type 1
|
|
Congenital Erythrocytosis Due To Erythropoietin Receptor Mutation
|
Congenital Polycythemia Due To Erythropoietin Receptor Mutation
|
|
Primary Congenital Erythrocytosis
|
Primary Familial Polycythemia
|
|
Erythrocytosis, Autosomal Dominant Benign
|
Erythrocytosis, Somatic
|
|
Autosomal Dominant Familial Erythrocytosis-1
|
Erythrocytosis Autosomal Dominant Benign
|
|
Familial Primary Polycythemia
|
Familial Erythrocytosis, 1
|
|
Erythrocytosis, Familial, Type 1
|
|
|
| Pulmonary Edema |
|
|
| Acquired Immunodeficiency Syndrome |
|
Acquired Immune Deficiency Syndrome
|
AIDS
|
|
Acquired Immune Deficiency
|
Acquired Immunodeficiency
|
|
Acquired Immunodeficiency Due To Protein Loss
|
|
|
| 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
|
|
|
| Diabetes Mellitus |
|
|
| Neuropathy |
|
Peripheral Neuropathy
|
Peripheral Neuropathies
|
|
|
| Erythema Infectiosum |
|
Fifth Disease
|
Slapped Cheek Syndrome
|
|
Parvovirus B19 Infection
|
|
|
| Pure Autonomic Failure |
|
Orthostatic Hypotension
|
Idiopathic Orthostatic Hypotension
|
|
Postural Hypotension
|
Bradbury-Eggleston Syndrome
|
|
Bradbury Eggleston Syndrome
|
Hypotension, Orthostatic
|
|
Hypotension, Postural
|
Paf
|
|
Pure Dysautonomia
|
Pure Idiopatic Dysautonomia
|
|
Hypotension Orthostatic
|
Primary Orthostatic Hypotension
|
|
Chronic Orthostatic Hypotension
|
|
|
| Analbuminemia |
|
ANALBA
|
Congenital Analbuminemia
|
|
Hypoalbuminemia
|
|
|
| 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
|
|
|
| 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
|
|
|
| Renal Fibrosis |
|
|
| 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
|
|
|
| Plethora Of Newborn |
|
|
| Retinal Detachment |
|
Retinal Detachments
|
Rhegmatogenous Retinal Detachment
|
|
Ruptured Retina With Detachment
|
Retinal Hole With Detachment
|
|
|
| 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
|
|
|
| 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
|
|
|
| Exudative Vitreoretinopathy 1 |
|
Retinopathy Of Prematurity
|
Retrolental Fibroplasia
|
|
EVR1
|
Criswick-Schepens Syndrome
|
|
Rop
|
Exudative Vitreoretinopathy, Familial, Autosomal Dominant
|
|
Fevr, Autosomal Dominant
|
Premature Retinopathy
|
|
Vitreoretinopathy, Exudative 1
|
Autosomal Dominant Familial Exudative Vitreoretinopathy
|
|
Fevr
|
Vitreoretinopathy, Exudative, Type 1
|
|
Retinopathy Of Prematurity Nos
|
Rlf- [Retrolental Fibroplasia]
|
|
Rop - [Retinopathy Of Prematurity]
|
Terry Syndrome
|
|
|
| Myelophthisic Anemia |
|
Myelophthisis
|
Anemia Leukoerythroblastic
|
|
Anemia, Leukoerythroblastic
|
Leukoerythroblastosis
|
|
Anemia, Myelophthisic
|
Leukoerythroblastic Anemia
|
|
|
| Beta-Thalassemia Intermedia |
|
|
| 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
|
|
|
| Progressive Myoclonus Epilepsy 9 |
|
Emp9
|
Pme Type 9
|
|
Progressive Myoclonic Epilepsy Due To Lmnb2 Deficiency
|
Progressive Myoclonus Epilepsy Type 9
|
|
|
| Viral Exanthem |
|
Viral Rash Nos
|
Virus Exanthema
|
|
Nonspecific Exanthematous Viral Infection
|
Nonspecific Viral Exanthem
|
|
Nonspecific Viral Rash
|
Viral Enanthema Nos
|
|
Viral Disease Characterised By Exanthem
|
Viral Exanthemata
|
|
Viral Exanthem, Unspecified
|
Viral Exanthema Nos
|
|
|
| Encephalomalacia |
|
|
| Splenic Sequestration |
|
|
| Periventricular Leukomalacia |
|
Leukomalacia, Periventricular
|
Pvl
|
|
Leukomalacia Periventricular
|
|
|
| Beta-Thalassemia Major |
|
Cooley'S Anemia
|
Cooley Anemia
|
|
Mediterranean Anemia
|
|
|
| Bone Disease |
|
Bone Diseases
|
Skeletal Disease
|
|
Skeletal Disorder
|
Disorder Of Skeletal System
|
|
|
| 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
|
|
|
| Type 1 Diabetes Mellitus 19 |
|
Diabetes Mellitus, Insulin-Dependent, 19
|
IDDM19
|
|
T1D19
|
Insulin-Dependent Diabetes Mellitus 19
|
|
|
| Parathyroid Gland Disease |
|
Parathyroid Diseases
|
Disease Of Parathyroid Glands
|
|
Parathyroid Disease
|
|
|
| Blood Group Incompatibility |
|
|
| 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
|
|
|
| Hypochromic Microcytic Anemia |
|
Anemia, Hypochromic Microcytic
|
Microcytic Hypochromic Anemia
|
|
|
| Vitamin B12 Deficiency |
|
Cobalamin Deficiency
|
Hypocobalaminemia
|
|
Vitamin B 12 Deficiency
|
Cyanocobalamin Deficiency
|
|
Deficiency Of Vitamin B12
|
|
|
| Uremic Neuropathy |
|
|
| Thalassemia Minor |
|
|
| Vitamin Metabolic Disorder |
|
|
| Hydrocephalus |
|
Hydrocephalus, Nonsyndromic, Autosomal Recessive
|
Hydrocephalus, X-Linked
|
|
Hydrocephalus Adverse Event
|
Hydrocephaly Nos
|
|
|
| Pheochromocytoma |
|
Pheochromocytoma, Susceptibility To
|
Phaeochromocytoma
|
|
Adrenal Gland Chromaffin Paraganglioma
|
Adrenal Gland Chromaffinoma
|
|
Adrenal Gland Paraganglioma
|
Adrenal Gland Pheochromocytoma
|
|
Chromaffin Paraganglioma Of The Adrenal Gland
|
Intraadrenal Paraganglioma
|
|
PCC
|
Chromaffin Cell Tumor
|
|
Medullary Chromaffinoma
|
Medullary Paraganglioma
|
|
Pheochromoblastoma
|
Pheochromocytomas
|
|
Chromaffin Cell Neoplasm
|
Pheochromocytoma, Malignant
|
|
|
| Congenital Hemolytic Anemia |
|
Anemia Hemolytic Congenital
|
Anemia, Hemolytic, Congenital
|
|
Congenital Hemolytic Anaemia
|
Hereditary Hemolytic Anaemia
|
|
Hereditary Hemolytic Anemia
|
|
|
| Heart Disease |
|
Heart Failure
|
Congenital Heart Disease
|
|
Heart Diseases
|
Congenital Heart Defects
|
|
Congenital Heart Defect
|
Heart Malformation
|
|
Congenital Anomaly Of Heart
|
Heart Defect
|
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
|
Heart Defects
|
Heart Disease, Congenital
|
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
| Retinal Degeneration |
|
|
| Nephrotic Syndrome |
|
Finnish Congenital Nephrotic Syndrome
|
Ns - [Nephrotic Syndrome]
|
|
Nephrosis Syndrome
|
Nephrosis Nos
|
|
Glomerular Lesion Nephrosis
|
|
|
| Renal Artery Disease |
|
Renal Vascular Disease
|
Vascular Disorder Of Kidney
|
|
Renal Vascular Disorder
|
|
|
| Blood Platelet Disease |
|
Platelet Disorder
|
Blood Platelet Disorders
|
|
Thrombocytopathy
|
Platelet Dysfunction
|
|
Platelet Disorders
|
Qualitative Platelet Deficiency
|
|
|
| Chronic Pyelonephritis |
|
|
| Renal Hypertension |
|
Hypertension Renal
|
Hypertension, Renal
|
|
|
| Epiglottis Cancer |
|
Epiglottic Cancer
|
Malignant Tumor Of Epiglottis
|
|
|
| Neovascular Glaucoma |
|
Glaucoma, Neovascular
|
Secondary Angle-Closure Glaucoma With Rubeosis
|
|
Glaucoma Neovascular
|
|
|
| Retinal Ischemia |
|
|
| Kidney Fibrosarcoma |
|
Fibrosarcoma Of The Kidney
|
|
|
| Myeloid And Lymphoid Neoplasms Associated With Pdgfra Rearrangement |
|
Myeloid/Lymphoid Neoplasm Associated With Pdgfra Rearrangement
|
Myeloid And Lymphoid Neoplasms With Pdgfra Rearrangement
|
|
|
| Blood Coagulation Disease |
|
Blood Coagulation Disorders
|
Coagulation Protein Disease
|
|
Inherited Blood Coagulation Disease
|
Postpartum Coagulation Defect
|
|
Postpartum Coagulation Defect With Delivery
|
Coagulation Protein Disorders
|
|
Puerperal Coagulopathy
|
|
|
| Blood Protein Disease |
|
Blood Protein Disorders
|
Blood Protein Disorder
|
|
|
| Carotid Artery Occlusion |
|
Occlusion And Stenosis Of Carotid Artery
|
|
|
| Bone Marrow Cancer |
|
Malignant Neoplasm Of Bone Marrow
|
Bone Marrow Neoplasm
|
|
Bone Marrow Tumor
|
Malignant Bone Marrow Tumor
|
|
Myeloproliferative Disorders
|
Bone Marrow Neoplasms
|
|
Myeloproliferative Disease
|
Chronic Myeloproliferative Disorder
|
|
|
| Perinatal Necrotizing Enterocolitis |
|
Necrotizing Enterocolitis
|
Enterocolitis Necrotizing
|
|
Enterocolitis, Necrotizing
|
Necrotizing Enterocolitis In Fetus Or Newborn
|
|
Perinatal Necrotising Enterocolitis
|
Pseudomembranous Enterocolitis In Newborn
|
|
Nec
|
|
|
| Mineral Metabolism Disease |
|
Mineral Metabolism Disorder
|
Disorder Of Mineral Metabolism
|
|
|
| Myocardial Infarction |
|
Heart Attack
|
Myocardial Infarction, Susceptibility To
|
|
Myocardial Infarction 1
|
Myocardial Infarction, Protection Against
|
|
Myocardial Infarction, Decreased Susceptibility To
|
Myocardial Infarction, Decreased
|
|
Myocardial Infarct
|
MCI1
|
|
Premature Myocardial Infarction
|
Myocardial Infarction, Susceptibility To, Type 1
|
|
|
| Metal Metabolism Disorder |
|
Metal Metabolism, Inborn Errors
|
Inborn Metal Metabolism Disorder
|
|
|
| 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]
|
|
|
| Erythrocytosis, Familial, 6 |
|
ECYT6
|
Erythrocytosis 6
|
|
Familial Erythrocytosis 6
|
Erythrocytosis, Beta-Globin Type
|
|
Polycythemia, Beta-Globin Type
|
Beta-Globin Type Erythrocytosis
|
|
Beta-Globin Type Polycythemia
|
|
|
| Anemia, Autoimmune Hemolytic |
|
Autoimmune Hemolytic Anemia
|
Idiopathic Autoimmune Hemolytic Anemia
|
|
Immuno-Hemolytic Anemia
|
Anemia, Hemolytic, Autoimmune
|
|
Autoimmune Haemolytic Anaemia
|
Autoimmune Hemolytic Anaemia
|
|
Acquired Autoimmune Hemolytic Anemia
|
Anemia Hemolytic Autoimmune
|
|
Familial Auto-Immune Hemolytic Anemia
|
Aha
|
|
Aiha
|
|
|
| Peripheral Vascular Disease |
|
Peripheral Arterial Disease
|
Arterial Occlusive Disease
|
|
Arterial Occlusive Diseases
|
Pad
|
|
Peripheral Vascular Diseases
|
Peripheral Occlusive Disease
|
|
Peripheral Arterial Diseases
|
Helicobacter Infections
|
|
|
| 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
|
|
|
| Hypertension, Essential |
|
Essential Hypertension
|
Hypertension
|
|
High Blood Pressure
|
Hypertension, Essential, Susceptibility To
|
|
Hypertensive Disease
|
Primary Hypertension
|
|
EHT
|
Hypertension, Salt-Sensitive Essential, Susceptibility To
|
|
Hyperpiesia
|
Idiopathic Hypertension
|
|
Hypertensive Disorder
|
Hypertension, Essential, Susceptibility To, 3
|
|
Hypertension, Essential 3
|
Hypertension, Essential, Salt-Sensitive
|
|
Hypertension, Essential, Susceptibility To, 6
|
Hypertension, Essential 6
|
|
Hypertension, Salt-Sensitive Essential
|
Hypertension, Susceptibility To
|
|
Hypertension, Essential, Susceptibility To, 4
|
Hypertension, Essential 4
|
|
Hypertension, Essential, Susceptibility To, 2
|
Hypertension, Essential 2
|
|
Hypertension, Essential, Susceptibility To, 1
|
Hypertension, Essential 1
|
|
Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
|
Htn
|
Vascular Hypertensive Disorder
|
|
Systemic Primary Arterial Hypertension
|
Hbp - [High Blood Pressure]
|
|
Systemic Arterial Hypertensive Disorder
|
Elevated Blood Pressure
|
|
Arterial Hypertension Nos
|
Hypertension Nos
|
|
Benign Hypertension
|
Systemic Arterial Hypertension
|
|
Systemic Hypertension
|
Artery Htn
|
|
Benign Htn
|
Vascular Htn
|
|
Vascular Hypertension
|
Cholesterol Hypertension
|
|
Cholesterol Htn
|
Idiopathic Htn
|
|
Malignant Hypertension
|
Malignant Htn
|
|
Raised Blood Pressure
|
Cardiovascular Hypertension
|
|
Primary Htn - [Hypertension]
|
High Arterial Tension
|
|
High Blood Pressure Disorder
|
Ht - [Hypertension]
|
|
Htn - [Hypertension]
|
Hypertensive Vascular Disease
|
|
Hypertensive Vascular Degeneration
|
|
|
| Conidiobolomycosis |
|
Infection By Conidiobolus
|
Rhinoentomophthoromycosis
|
|
Entomophthoromycosis Conidiobolae
|
|
|
| Esophagus Carcinoma In Situ |
|
Carcinoma In Situ Of Esophagus
|
Carcinoma In Situ Of Oesophagus
|
|
Oesophagus Carcinoma In Situ
|
Severe Esophageal Dysplasia
|
|
Stage 0 Carcinoma Of The Esophagus
|
Stage 0 Carcinoma Of The Oesophagus
|
|
Severe Oesophageal Dysplasia
|
|
|
| Tremor, Hereditary Essential, 2 |
|
ETM2
|
Essential Tremor 2
|
|
Essential Tremor, Hereditary, 2
|
Hereditary Essential Tremor 2
|
|
Tremor Hereditary Essential, 2
|
|
|
| Cystic Kidney Disease |
|
Renal Cyst
|
Simple Renal Cyst
|
|
Kidney Cysts
|
Kidney Diseases, Cystic
|
|
Renal Cysts
|
Kidney Cyst
|
|
Cystic Kidney
|
Congenital Cystic Kidney Disease
|
|
Cystic Kidney Diseases
|
Bosniak 1 Cyst
|
|
|
| Ceftazidime Allergy |
|
Fortaz Allergy
|
Tazicef Allergy
|
|
|
| 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
|
|
|
| Fallopian Tube Clear Cell Adenocarcinoma |
|
Clear Cell Carcinoma Of The Fallopian Tube
|
|
|
| Patent Ductus Arteriosus 1 |
|
Patent Ductus Arteriosus
|
PDA1
|
|
Pda
|
Ductus Arteriosus, Patent
|
|
Patent Ductus Arteriosus, Susceptibility To
|
Patent Ductus Botalli
|
|
Patency Of The Ductus Arteriosus
|
Patent Ductus Arteriosus Familial
|
|
Ductus Arteriosus Patent
|
Patent Ductus Arteriosus - Persisting Type
|
|
|
| Bilirubin Metabolic Disorder |
|
Hyperbilirubinemia
|
Hereditary Hyperbilirubinemia
|
|
Hyperbilirubinemia, Hereditary
|
Hyperbilirubinaemia
|
|
|
| Intracranial Berry Aneurysm |
|
Familial Aneurysmal Subarachnoid Hemorrhage
|
Familial Berry Aneurysm
|
|
Familial Intracranial Saccular Aneurysm
|
Saccular Cerebral Aneurysm
|
|
Aneurysm, Intracranial Berry
|
Aneurysmal Subarachnoid Hemorrhage
|
|
Aneurysm, Intracranial Berry, 1
|
|
|
| Autosomal Dominant Polycystic Kidney Disease |
|
Polycystic Kidney Disease, Adult Type
|
Adpkd
|
|
Polycystic Kidney Diseases
|
Polycystic Kidney, Autosomal Dominant
|
|
Congenital Biliary Ectasias
|
Polycystic Kidney And Hepatic Disease 1
|
|
Polycystic Kidney Disease, Autosomal Dominant
|
Kidney, Polycystic, Disease, Autosomal Dominant
|
|
Adult Polycystic Kidney Disease
|
Polycystic Kidney, Adult Type
|
|
Apckd - [Autosomal Polycystic Kidney Disease]
|
|
|
| Cerebral Palsy |
|
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
|
Palsy Cerebral
|
Palsy, Cerebral
|
|
Cerebral Palsy, Mixed
|
|
|
| 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
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Eye Disease |
|
Eye Diseases
|
Abnormality Of The Eye
|
|
Toxoplasma Oculopathy
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
