| Diseases |
Alias |
|
| Anemia, Nonspherocytic Hemolytic, Due To G6pd Deficiency |
|
Favism
|
Favism, Susceptibility To
|
|
Hemolytic Anemia, G6pd Deficient
|
Class I Glucose-6-Phosphate Dehydrogenase Deficiency
|
|
Class I G6pd Deficiency
|
Severe Hemolytic Anemia Due To G6pd Deficiency
|
|
Anemia, Non-Spherocytic Hemolytic, Due To G6pd Deficiency
|
NSHA
|
|
G6pd Deficient Hemolytic Anemia
|
|
|
| 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
|
|
|
| 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
|
|
|
| Congenital Hemolytic Anemia |
|
Anemia Hemolytic Congenital
|
Anemia, Hemolytic, Congenital
|
|
Congenital Hemolytic Anaemia
|
Hereditary Hemolytic Anaemia
|
|
Hereditary Hemolytic Anemia
|
|
|
| Neonatal Jaundice |
|
Neonatal Hyperbilirubinemia
|
Neonatal Icterus
|
|
Jaundice Neonatal
|
Jaundice, Neonatal
|
|
Hyperbilirubinemia, Neonatal
|
|
|
| Blackwater Fever |
|
Black Water Fever
|
Hemoglobinuric, Malaria
|
|
Malarial Hemoglobinuria
|
|
|
| Plasmodium Vivax Malaria |
|
Malaria, Vivax
|
Malaria By Plasmodium Vivax
|
|
Vivax Malaria
|
Malaria Vivax
|
|
|
| Kernicterus |
|
Bilirubin Encephalopathy
|
Hyperbilirubinemic Encephalopathy
|
|
Kernicterus Spectrum Disorder
|
|
|
| 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
|
|
|
| Blood Group Incompatibility |
|
|
| Methemoglobinemia |
|
|
| Plasmodium Falciparum Malaria |
|
Falciparum Malaria
|
Malaria, Falciparum
|
|
Malaria Fever, Subtertian
|
Malignant Tertian Fever
|
|
Malaria Falciparum
|
Cerebral Malaria Nos
|
|
Cerebral Malaria
|
|
|
| Pyruvate Kinase Deficiency Of Red Cells |
|
Pyruvate Kinase Deficiency
|
Pk Deficiency
|
|
Pyruvate Kinase Deficiency Of Erythrocyte
|
Hemolytic Anemia Due To Red Cell Pyruvate Kinase Deficiency
|
|
Pyruvate Kinase Deficiency Of Erythrocytes
|
Pkd
|
|
PKRD
|
Hereditary Non-Spherocytic Hemolytic Anemia Due To Pyruvate Kinase Deficiency
|
|
Hnsha
|
Pyruvate Kinase-Deficient Hemolytic Anemia
|
|
Red Cell Pyruvate Kinase Deficiency
|
Deficiency Of Pyruvate Kinase
|
|
Anemia, Hemolytic, Congenital Nonspherocytic
|
|
|
| Senile Cataract |
|
|
| Acquired Methemoglobinemia |
|
Drug-Induced Methemoglobinemia
|
Methemoglobinemia Acquired
|
|
|
| Color Blindness |
|
Color Vision Defect
|
Blindness Color
|
|
Colour Blindness
|
Colour Vision Deficiency
|
|
Color Vision Deficiency
|
Color Vision Defects
|
|
Defective Color Vision
|
Vision Defect, Color
|
|
Color-Vision Disease
|
Dyschromatopsia
|
|
|
| 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
|
|
|
| 6-Phosphogluconate Dehydrogenase Deficiency |
|
|
| Alpha-Thalassemia |
|
Alpha Thalassemia
|
Alpha Thalassaemia
|
|
Alpha Plus Thalassemia
|
Thalassemia, Alpha-
|
|
Thalassemias, Alpha-
|
A-Thalassemia
|
|
Α-Thalassemia
|
A-THAL
|
|
Thalassemia
|
Alpha Thalassaemia Syndrome
|
|
|
| Plasmodium Ovale Malaria |
|
Ovale Malaria
|
Malariaby Plasmodium Ovale
|
|
|
| Gilbert Syndrome |
|
Gilbert Disease
|
Gilbert'S Disease
|
|
Gilbert'S Syndrome
|
Cholemia, Familial
|
|
Familial Nonhemolytic Jaundice
|
Meulengracht Syndrome
|
|
Gilbert Syndrome, Susceptibility To
|
Hyperbilirubinemia, Gilbert Type
|
|
Hblrg
|
Hyperbilirubinemia, Arias Type
|
|
Hyperbilirubinemia I
|
Constitutional Hyperbilirubinemia
|
|
Gilbert-Meulengracht Syndrome
|
Hereditary Nonhemolytic Jaundice
|
|
Hyperbilirubinemia Arias Type
|
Hyperbilirubinemia Type 1
|
|
Constitutional Liver Dysfunction
|
Gilbert-Lereboullet Syndrome
|
|
Hyperbilirubinemia 1
|
Unconjugated Benign Bilirubinemia
|
|
GILBS
|
Gilberts Syndrome
|
|
Familial Nonhaemolytic Jaundice
|
Constitutional Hyperbilirubinaemia
|
|
Hereditary Nonhaemolytic Bilirubinaemia
|
Familial Nonhaemolytic Bilirubinaemia
|
|
Idiopathic Hyperbilirubinaemia
|
Icterus Intermittens Juvenilis
|
|
Chronic Intermittent Juvenile Jaundice
|
Low-Grade Chronic Hyperbilirubinaemia Syndrome
|
|
Benign Unconjugated Bilirubinaemia Syndrome
|
Hereditary Nonhaemolytic Jaundice
|
|
Idiopathic Unconjugated Hyperbilirubinaemia
|
Gilbert--Lereboullet Syndrome
|
|
Constitutional Hepatic Dysfunction
|
Meulengracht Icterus
|
|
Cholaemia Familiaris Simplex
|
Familial Cholaemia
|
|
Congenital Familial Cholaemia
|
Physiologic Cholaemia
|
|
Hyperbilirubinaemia Type 1
|
Gilbert Cholaemia
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| 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
|
|
|
| Phenylketonuria |
|
Phenylalanine Hydroxylase Deficiency
|
PKU
|
|
Pah Deficiency
|
Folling Disease
|
|
Maternal Phenylketonuria
|
Phenylketonurias
|
|
Oligophrenia Phenylpyruvica
|
Hyperphenylalaninemia, Non-Pku Mild
|
|
Folling'S Disease
|
Phenylalaninemia
|
|
Mild Phenylketonuria
|
Mild Pku
|
|
Variant Pku
|
Variant Phenylketonuria
|
|
Mpku
|
Deficiency Disease, Phenylalanine Hydroxylase
|
|
Phenylketonuria, Maternal
|
Phenylalanine Hydroxylase Deficiency Disease
|
|
Hyperphenylalaninemic Embryopathy
|
Maternal Pku
|
|
Maternal Hyperphenylalaninemia
|
Phenylketonuric Embryopathy
|
|
Hyperphenylalaninemia
|
HPA
|
|
Non-Phenylketonuria Hyperphenylalaninemia
|
NON-PKU HPA
|
|
Phenylketonuria Maternal
|
Classical Phenylketonuria
|
|
Hyperphenylalaninaemia
|
Pku - [Phenylketonuria]
|
|
|
| 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]
|
|
|
| Glutathione Synthetase Deficiency |
|
5-Oxoprolinuria
|
Pyroglutamic Aciduria
|
|
Pyroglutamicaciduria
|
Glutathione Synthetase Deficiency With 5-Oxoprolinuria
|
|
GSSD
|
Oxoprolinase Deficiency
|
|
5-Oxoprolinemia
|
Deficiency Of Glutathione Synthase
|
|
Deficiency Of Glutathione Synthetase
|
Pyroglutamic Acidemia
|
|
GSS DEFICIENCY
|
Gluthathione Synthetase Deficiency
|
|
5-Oxoprolinase Deficiency
|
|
|
| Galactosemia I |
|
Galactosemia
|
Galt Deficiency
|
|
Classic Galactosemia
|
Galactose-1-Phosphate Uridylyltransferase Deficiency
|
|
Galactose-1-Phosphate Uridyltransferase Deficiency
|
GALAC1
|
|
Galactosemia, Classic
|
Galactosemia Type 1
|
|
Galactosemias
|
Classical Galactosemia
|
|
Galactosaemia
|
Galactose Intolerance
|
|
Epimerase Deficiency Galactosemia
|
Galactokinase Deficiency Disease
|
|
Galactose Epimerase Deficiency
|
Galactose-1-Phosphate Uridyl-Transferase Deficiency Disease
|
|
Gale Deficiency
|
Galk Deficiency
|
|
Udp-Galactose-4-Epimerase Deficiency Disease
|
Utp Hexose-1-Phosphate Uridylyltransferase Deficiency
|
|
Galactosemia 1
|
Galactosemia, Duarte Variant
|
|
Deficiency Of Galactokinase
|
Udpglucose 4-Epimerase Deficiency Disease
|
|
Classical Galactosaemia
|
Galput Deficiency - [Galactose-4-Phosphate Uridyltransferase] Deficiency
|
|
Classic Galactosaemia
|
Deficiency Of Hexose-1-Phosphate Uridylyltransferase
|
|
Deficiency Of Udpglucose-Hexose-1-Phosphate Uridylyltransferase
|
Deficiency Of Galactose-1-Phosphate Uridylyltransferase
|
|
Galactose-1-Phosphate Uridyl Transferase Deficiency
|
Transferase Deficiency Galactosemia
|
|
Deficiency Of Uridyl Transferase
|
Deficiency Of Utp-Hexose-1-Phosphate Uridylyltransferase
|
|
Utp-Hexose-1-Phosphate Uridyltransferase Deficiency
|
|
|
| Cutaneous Leishmaniasis |
|
Diffuse Cutaneous Leishmaniasis
|
Asian Desert Cutaneous Leishmaniasis
|
|
Leishmaniasis, Cutaneous
|
Leproid Leishmaniasis
|
|
Leishmaniasis Diffuse Cutaneous
|
Leishmaniasis Cutaneous
|
|
Ethiopian Cutaneous Leishmaniasis
|
Old World Cutaneous Leishmaniasis
|
|
|
| Hemoglobinopathy |
|
|
| 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
|
|
|
| Microcytic Anemia |
|
Iron-Refractory Iron Deficiency Anemia
|
|
|
| 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
|
|
|
| Hemoglobinuria |
|
|
| Bilirubin Metabolic Disorder |
|
Hyperbilirubinemia
|
Hereditary Hyperbilirubinemia
|
|
Hyperbilirubinemia, Hereditary
|
Hyperbilirubinaemia
|
|
|
| Hereditary Elliptocytosis |
|
Congenital Elliptocytosis
|
Ovalocytosis
|
|
Elliptocytosis, Hereditary
|
He
|
|
Elliptocytosis Hereditary
|
Congenital Ovalocytosis
|
|
Elliptocytosis
|
Hereditary Elliptocytosis With Infantile Poikilocytosis
|
|
Hereditary Ovalocytosis
|
Oval Erythrocytosis
|
|
He - [Hereditary Elliptocytosis]
|
Elliptocytosis Anaemia
|
|
|
| Iron Deficiency Anemia |
|
Iron-Deficiency Anemia
|
Fe Deficiency Anaemia
|
|
Ida - [Iron Deficiency Anemia]
|
Fe - [Iron] Deficiency Anemia Nos
|
|
|
| Diabetic Cataract |
|
|
| 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
|
|
|
| Chronic Granulomatous Disease |
|
Cgd
|
Granulomatous Disease, Chronic
|
|
Autosomal Recessive Chronic Granulomatous Disease
|
X-Linked Chronic Granulomatous Disease
|
|
Bridges-Good Syndrome
|
Congenital Dysphagocytosis
|
|
Quie Syndrome
|
Chronic Septic Granulomatosis
|
|
Chronic Granulomatous Disorder
|
Granulomatous Disease Chronic
|
|
Granulomatous Disease, Chronic, X-Linked
|
|
|
| Viral Hepatitis |
|
Animal Viral Hepatitis
|
Hepatitis, Viral, Animal
|
|
Human Viral Hepatitis
|
Viral Hepatitis With Hepatic Coma
|
|
|
| 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
|
|
|
| Parotitis |
|
|
| Cardiac Arrest |
|
Cardiopulmonary Arrest
|
Circulatory Arrest
|
|
Heart Arrest
|
|
|
| Histiocytosis-Lymphadenopathy Plus Syndrome |
|
H Syndrome
|
Histiocytosis With Joint Contractures And Sensorineural Deafness
|
|
Faisalabad Histiocytosis
|
Shml
|
|
Hjcd
|
Rosai-Dorfman Disease
|
|
Pigmented Hypertrichosis With Insulin-Dependent Diabetes Mellitus
|
Phid
|
|
Sinus Histiocytosis And Massive Lymphadenopathy
|
Familial Rosai-Dorfman Disease
|
|
Slc29a3 Spectrum Disorder
|
Sinus Histiocytosis With Massive Lymphadenopathy
|
|
Histiocytosis And Lymphadenopathy With Or Without Cutaneous, Cardiac, And/Or Endocrine Features, Joint Contractures, And/Or Deafness
|
Hyperpigmentation, Cutaneous, With Hypertrichosis, Hepatosplenomegaly, Heart Anomalies, And Hypogonadism With Or Without Hearing Loss
|
|
Rosai-Dorfman Disease, Familial
|
Cutaneous Hyperpigmentation With Hypertrichosis, Hepatosplenomegaly, Heart Anomalies, And Hypogonadism With Or Without Hearing Loss
|
|
Histiocytosis And Lymphadenopathy With Or Without Cutaneous, Cardiac, And/Or Endocrine Features, Joint Contractures And/Or Deafness
|
Rdd
|
|
Rosaï-Dorfman Disease
|
Slc29a3 Disorder
|
|
Destombes-Rosai-Dorfman Disease
|
Rosai-Dorfman-Destombes Disease
|
|
HLAS
|
Cutaneous Hyperpigmentation With Hypertrichosis Hepatosplenomegaly Heart Anomalies And Hypogonadism With Or Without Hearing Loss
|
|
Histiocytosis And Lymphadenopathy With Or Without Cutaneous Cardiac And/Or Endocrine Features Joint Contractures And/Or Deafness
|
H Disease
|
|
Sinus Histiocytosis
|
|
|
| Boutonneuse Fever |
|
Mediterranean Spotted Fever
|
African Tick Typhus
|
|
Boutonneuse Disease
|
Conor And Bruch'S Disease
|
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Kenya Fever
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Kenya Tick Typhus
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Kenyan Tick Typhus
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Marseilles Fever
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Mediterranean Tick Fever
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Rickettsia Conorii Spotted Fever
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South African Tick-Bite Fever
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African Tick Bite Fever
|
|
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| Rh Isoimmunization |
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Rh Incompatibility Affecting Management Of Mother
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| Pericarditis |
|
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| Hepatitis A |
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Viral Hepatitis A
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Viral Hepatitis, Type A
|
|
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| Pigmentation Disease |
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Pigmentation Disorders
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Skin Pigmentation Disorder
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|
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| Toxoplasmosis |
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Disseminated Toxoplasmosis
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Multisystemic Disseminated Toxoplasmosis
|
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Acquired Toxoplasmosis
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Toxoplasmosis Disease Or Disorder
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Infection By Toxoplasma Gondii
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Toxoplasmal
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Toxoplasma
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|
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| Trimethoprim Allergy |
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Primsol Allergy
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Proloprim Allergy
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Tmp Allergy
|
|
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| Paroxysmal Nocturnal Hemoglobinuria |
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Marchiafava-Micheli Disease
|
Pnh
|
|
Hemoglobinuria, Paroxysmal
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Marchiafava-Micheli Syndrome
|
|
Paroxysmal Hemoglobinuria Nocturnal
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Nocturnal Haemoglobinuria
|
|
Nocturnal Paroxysmal Haematuria
|
Nocturnal Paroxysmal Haemoglobinaemia
|
|
|
| Iron Metabolism Disease |
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Iron Deficiency
|
Iron Disorder
|
|
Iron Metabolism Disorders
|
Disorder Of Iron Metabolism
|
|
Iron
|
Fe Deficiency
|
|
Iron Storage Disease
|
Iron Storage Disorder
|
|
|
| Sulfonamide Allergy |
|
|
| Parasitic Protozoa Infectious Disease |
|
Protozoan Infections
|
Mastigophora Infectious Disease
|
|
Sarcomastigophora Infectious Disease
|
|
|
| Cataract |
|
Cataracts
|
Cat - [Cataract]
|
|
Cataract Form
|
Lens Opacity
|
|
Lens Opacities
|
|
|
| Asbestosis |
|
Idiopathic Interstitial Pneumonitis - From Asbestos Exposure
|
Pulmonary Fibrosis - From Asbestos Exposure
|
|
|
| Congenital Hypothyroidism |
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Cretinism
|
Neonatal Hypothyroidism
|
|
Ch
|
Cht
|
|
Congenital Myxedema
|
Myxedema, Congenital
|
|
Endemic Cretinism
|
Congenital Iodine-Deficiency Syndrome
|
|
Fetal Iodine Deficiency Syndrome
|
Congenital Iodine-Deficiency Hypothyroidism Nos
|
|
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| 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
|
|
|
| Hydrops Of Gallbladder |
|
|
| Holoprosencephaly 1 |
|
Arhinencephaly
|
HPE1
|
|
Cyclopia
|
Holoprosencephaly, Familial Alobar
|
|
Hpe, Familial
|
Hpec
|
|
Demyer Sequence
|
Holoprosencephaly-1
|
|
|
| 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
|
|
|
| Gallbladder Melanoma |
|
Malignant Melanoma Of Gallbladder
|
|
|
| Respiratory Failure |
|
Acute Respiratory Failure
|
Chronic Respiratory Failure
|
|
Respiratory Insufficiency
|
Acute-On-Chronic Respiratory Failure
|
|
Respiratory Disease
|
Acute And Chronic Respiratory Failure
|
|
Respiratory Insufficiency/Failure
|
Chronic Respiratory Disease
|
|
Pulmonary Valve Insufficiency
|
Chronic Disease Of Respiratory System
|
|
Respiration Disorders
|
Respiratory Tract Diseases
|
|
Lung Failure Nos
|
Pulmonary Failure
|
|
Arf - [Acute Respiratory Failure]
|
Acute Respiratory Insufficiency
|
|
Acute Pulmonary Insufficiency
|
Acute Respiration Failure
|
|
Chronic Respiration Failure
|
|
|
| Diabetes Mellitus |
|
|
| 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
|
|
|
