| Diseases |
Alias |
|
| Hemophilia B |
|
Christmas Disease
|
Factor Ix Deficiency
|
|
F9 Deficiency
|
HEMB
|
|
Plasma Thromboplastin Component Deficiency
|
Congenital Factor Ix Deficiency
|
|
Mild Hemophilia B
|
Severe Hemophilia B
|
|
Congenital Factor Ix Disorder
|
Deficiency, Functional Factor Ix
|
|
Hem B
|
Mild Congenital F9 Deficiency
|
|
Mild Congenital Factor Ix Deficiency
|
Moderate Hemophilia B
|
|
Moderate Congenital F9 Deficiency
|
Moderate Congenital Factor Ix Deficiency
|
|
Severe Congenital F9 Deficiency
|
Severe Congenital Factor Ix Deficiency
|
|
Bleeding Disorder In Hemophilia B Carriers
|
Congenital F9 Deficiency
|
|
Recessive X-Linked Hemophilia B
|
|
|
| Thrombophilia, X-Linked, Due To Factor Ix Defect |
|
THPH8
|
Deep Venous Thrombosis, Protection Against
|
|
X-Linked Thrombophilia Due To Factor Ix Defect
|
Thrombophilia, X-Linked, Due To Factor 9 Defect
|
|
Thrombophilia 8, X-Linked, Due To Factor Ix Defect
|
|
|
| Warfarin Sensitivity, X-Linked |
|
Coumarin Sensitivity, X-Linked
|
X-Linked Warfarin Sensitivity
|
|
Warfarin Sensitivity
|
WARFS
|
|
|
| Hemophilia B Leyden |
|
F9 Deficiency, Leyden Type
|
Factor Ix Deficiency, Leyden Type
|
|
|
| Hemophilia A |
|
Factor Viii Deficiency
|
Haemophilia A
|
|
Mild Hemophilia A
|
HEMA
|
|
Hemophilia, Classic
|
Classic Hemophilia
|
|
Factor 8 Deficiency
|
Severe Hemophilia A
|
|
Classical Hemophilia
|
Hem A
|
|
Hemophilia A, Congenital
|
Mild Congenital F8 Deficiency
|
|
Mild Congenital Factor Viii Deficiency
|
Severe Congenital F8 Deficiency
|
|
Severe Congenital Factor Viii Deficiency
|
Moderate Hemophilia A
|
|
Moderate Congenital F8 Deficiency
|
Moderate Congenital Factor Viii Deficiency
|
|
Bleeding Disorder In Hemophilia A Carriers
|
Congenital F8 Deficiency
|
|
Congenital Fviii Deficiency
|
Congenital Factor Viii Deficiency
|
|
Mild Hereditary Factor Viii Deficiency Disease
|
Severe Hereditary Factor Viii Deficiency Disease
|
|
Ahg - [Antihaemophilic Globulin] Deficiency
|
Ahg - [Antihaemophilic Globulin] Deficiency Disease
|
|
Congenital Factor Viii Disorder
|
Sex-Linked Factor Viii Deficiency
|
|
Antihaemophilic Globulin Deficiency
|
Classic Haemophilia
|
|
Familial Haemophilia
|
Haemophilia
|
|
Hereditary Haemophilia
|
Subhaemophilia
|
|
Haemophilia Nos
|
|
|
| Factor Viii Deficiency |
|
Autosomal Hemophilia A
|
Hemophilia A
|
|
Autosomal Factor Viii Deficiency
|
Classic Hemophilia A
|
|
Congenital Factor Viii Disorder
|
Subhemophilia
|
|
Factor 8 Deficiency, Congenital
|
Factor Viii
|
|
|
| Hemophilia |
|
Haemophilia
|
Hemophilia, Familial
|
|
Hemophilia, Hereditary
|
Hemophilia A
|
|
Hemophilia, Nos
|
|
|
| Thrombophilia |
|
|
| Hemarthrosis |
|
Haemarthrosis Of Shoulder Joint
|
Haemarthrosis Of The Ankle And Foot
|
|
Haemarthrosis Of The Pelvic Region And Thigh
|
Hemarthrosis Involving Ankle And Foot
|
|
Hemarthrosis Involving Forearm
|
Hemarthrosis Involving Hand
|
|
Hemarthrosis Involving Lower Leg
|
Hemarthrosis Involving Pelvic Region And Thigh
|
|
Hemarthrosis Involving Shoulder Region
|
Hemarthrosis Involving Upper Arm
|
|
Hemarthrosis Of Ankle And/Or Foot
|
Hemarthrosis Of Forearm
|
|
Hemarthrosis Of Hand
|
Hemarthrosis Of Lower Leg
|
|
Hemarthrosis Of Shoulder
|
Hemarthrosis Of Shoulder Region
|
|
Hemarthrosis Of The Ankle And Foot
|
Hemarthrosis Of The Ankle And/Or Foot
|
|
Hemarthrosis Of The Forearm
|
Hemarthrosis Of The Hand
|
|
Hemarthrosis Of The Lower Leg
|
Hemarthrosis Of The Pelvic Region And Thigh
|
|
Hemarthrosis Of The Shoulder Region
|
Hemarthrosis Of The Upper Arm
|
|
Hemarthrosis Of Upper Arm
|
|
|
| Factor Xi Deficiency |
|
Plasma Thromboplastin Antecedent Deficiency
|
Rosenthal Syndrome
|
|
Pta Deficiency
|
Hemophilia C
|
|
Rosenthal Factor Deficiency
|
F11 Deficiency
|
|
Congenital Factor Xi Deficiency
|
Hereditary Factor Xi Deficiency Disease
|
|
Haemophilia C
|
Factor Xi Deficiency, Autosomal Dominant
|
|
Rosenthal'S Disease
|
Factor 11 Deficiency
|
|
Factor Xi
|
Factor Xi Deficiency, Autosomal Recessive
|
|
Factor Xi Deficiency, Congenital
|
FA11D
|
|
Thromboplastin Antecedent Deficiency
|
Pta - [Plasma Thromboplastin Antecedent] Deficiency
|
|
Congenital Factor Xi Deficiency Disease
|
Rosenthal Disease
|
|
|
| Factor Vii Deficiency |
|
Hypoproconvertinemia
|
F7 Deficiency
|
|
Congenital Proconvertin Deficiency
|
Congenital Factor Vii Deficiency
|
|
Factor 7 Deficiency
|
Deficiency, Stable
|
|
Proconvertin Deficiency
|
Prothrombin Conversion Accelerator Deficiency
|
|
Serum Prothrombin Conversion Accelerator Deficiency
|
Proconvertin Deficiency, Congenital
|
|
FA7D
|
Stable Disease
|
|
Deficiency, Factor Vii
|
|
|
| Factor X Deficiency |
|
Stuart-Prower Factor Deficiency
|
F10 Deficiency
|
|
Congenital Stuart Factor Deficiency
|
Factor X Deficiency, Congenital
|
|
Congenital Factor X Deficiency
|
Disease, Stuart-Prower
|
|
Stuart Factor Deficiency, Congenital
|
FA10D
|
|
Factor 10 Deficiency
|
Deficiency, Factor X
|
|
Hereditary Factor X Deficiency Disease
|
Deficiency Of Factor X
|
|
Stuart Deficiency Disease
|
Stuart Prower Deficiency
|
|
Stuart-Prower Disease
|
|
|
| Thrombosis |
|
Thrombosis Of Blood Vessel
|
|
|
| Hemorrhagic Disease |
|
Hemorrhagic Disorders
|
Hemorrhagic Diathesis
|
|
Hemorrhagic Diseases
|
Bleeding Tendency
|
|
Acquired Coagulation Factor Inhibitor Disorder
|
Acquired Inhibitor Of Coagulation
|
|
Antithrombinaemia
|
Antithromboplastinogenaemia
|
|
Circulating Anticoagulant Disorder
|
Haemorrhagic Disorder Due To Antithrombinaemia
|
|
Haemorrhagic Disorder Due To Excess Administered Heparin
|
Antithromboplastinaemia
|
|
Haemorrhagic Disorder Due To Hyperheparinemia
|
|
|
| Protein C Deficiency |
|
Hereditary Thrombophilia Due To Protein C Deficiency
|
Proc Deficiency
|
|
Congenital Thrombotic Disease, Due To Protein C Deficiency
|
|
|
| Cardiac Tamponade |
|
Pericardial Tamponade
|
Rose'S Tamponade
|
|
|
| Von Willebrand'S Disease |
|
Von Willebrand Disease
|
Von Willebrand Disorder
|
|
Vascular Pseudohemophilia
|
Hereditary Von Willebrand Disease
|
|
Vwd
|
Vascular Hemophilia
|
|
Von Willebrand'S-Jurgens' Disease
|
Von Willebrand-Jrgens Disease
|
|
Von Willebrand Factor Deficiency
|
Von Willebrand Factor, Deficiency
|
|
Angiohemophilia
|
Von Willebrand'S Factor Deficiency
|
|
Von Willebrand Diseases
|
Factor Viii Deficiency With Vascular Defect
|
|
Vascular Haemophilia
|
Willebrand Jurgen Thrombopathy
|
|
Pseudohaemophilia
|
Minot-Von Willebrand-Jurgen Disease
|
|
Angiohaemophilia
|
Angiohaemophilia A
|
|
Angiohaemophilia B
|
|
|
| Factor V Deficiency |
|
Parahemophilia
|
Labile Factor Deficiency
|
|
Proaccelerin Deficiency
|
Owren Disease
|
|
Owren Parahemophilia
|
Quebec Platelet Disorder
|
|
Deficiency, Labile
|
Hereditary Hypoproaccelerinaemia
|
|
Owren'S Disease
|
Congenital Factor V Deficiency
|
|
FA5D
|
Factor 5 Deficiency
|
|
Deficiency, Factor V
|
|
|
| Arthropathy |
|
Ankylosis Of Ankle And Foot Joint
|
Ankylosis Of Forearm Joint
|
|
Ankylosis Of Hand Joint
|
Ankylosis Of Joint Of Ankle And/Or Foot
|
|
Ankylosis Of Joint Of Forearm
|
Ankylosis Of Joint Of Hand
|
|
Ankylosis Of Joint Of Lower Leg
|
Ankylosis Of Joint Of Multiple Sites
|
|
Ankylosis Of Joint Of Pelvic Region And Thigh
|
Ankylosis Of Joint Of Shoulder Region
|
|
Ankylosis Of Joint Of Upper Arm
|
Ankylosis Of Lower Leg Joint
|
|
Ankylosis Of Multiple Joints
|
Ankylosis Of Upper Arm Joint
|
|
Infectious Arthropathy
|
Joint Ankylosis Of The Ankle And Foot
|
|
Joint Ankylosis Of The Ankle And/Or Foot
|
Joint Ankylosis Of The Forearm
|
|
Joint Ankylosis Of The Hand
|
Joint Ankylosis Of The Lower Leg
|
|
Joint Ankylosis Of The Pelvic Region And Thigh
|
Joint Ankylosis Of The Shoulder Region
|
|
Joint Ankylosis Of The Upper Arm
|
Joint Diseases
|
|
Joint Disease
|
Arthropathy Associated With Infection
|
|
|
| Disseminated Intravascular Coagulation |
|
Defibrination Syndrome
|
Dic
|
|
Diffuse Or Disseminated Intravascular Coagulation
|
Fibrinolytic Purpura
|
|
Consumption Coagulopathy
|
Diffuse Intravascular Coagulation
|
|
Dic - [Disseminated Intravascular Coagulation]
|
Disseminated Intravascular Coagulopathy
|
|
Fibrinolysis Nos
|
Thrombolytic Purpura
|
|
|
| Factor Xii Deficiency |
|
Hageman Factor Deficiency
|
Haf Deficiency
|
|
Factor Xii Deficiency Disease
|
F12 Deficiency
|
|
Deficiency, Hageman
|
Coagulation Factor 12 Deficiency
|
|
Factor 12 Deficiency
|
Congenital Factor Xii Deficiency
|
|
Congenital Hageman Factor Deficiency
|
FA12D
|
|
Factor Xii
|
Deficiency, Factor Xii
|
|
|
| Sneddon Syndrome |
|
Livedo Reticularis And Cerebrovascular Accidents
|
SNDNS
|
|
Ehrmann-Sneddon Syndrome
|
Livedo Racemosa-Cerebrovascular Accident Syndrome
|
|
Livedo Reticularis-Cerebrovascular Accident Syndrome
|
Sneddon'S Syndrome
|
|
Idiopathic Livedo Reticularis With Systemic Involvement
|
Cerebro-Vascular Lesions And Livedo Reticularis
|
|
Livedo Racemosa And Cerebrovascular Accidents
|
|
|
| Atrial Fibrillation |
|
A-Fib
|
Fibrillation, Atrial
|
|
Af - [Atrial Fibrillation]
|
Rapid Atrial Fibrillation
|
|
A Fib - [Atrial Fibrillation]
|
|
|
| Immunoglobulin Light Chain Amyloidosis |
|
Al Amyloidosis
|
Primary Amyloidosis
|
|
Primary Systemic Amyloidosis
|
Light Chain Amyloidosis
|
|
Amyloidosis Al
|
Amyloidosis Primary Systemic
|
|
Primary Al Amyloidosis
|
Primary Systemic Al Amyloidosis
|
|
Systemic Al Amyloidsis
|
Systemic Al Amyloidosis
|
|
Light-Chain Amyloidosis
|
Alys Amyloidosis
|
|
Familial Amyloid Nephropathy Due To Lysozyme Variant
|
Familial Renal Amyloidosis Due To Lysozyme Variant
|
|
Hereditary Amyloid Nephropathy Due To Lysozyme Variant
|
Hereditary Renal Amyloidosis Due To Lysozyme Variant
|
|
Lysozyme Amyloidosis
|
Amyloidosis Primary
|
|
Immunoglobulin Deposition Disease
|
Immunoglobulinic Amyloidosis
|
|
Amyloid Al
|
|
|
| Pulmonary Embolism |
|
Pulmonary Artery Embolism
|
Pulmonary Embolus
|
|
Pulmonary Emboli
|
|
|
| Thrombophilia Due To Activated Protein C Resistance |
|
Activated Protein C Resistance
|
Apc Resistance
|
|
THPH2
|
Thrombophilia Due To Deficiency Of Activated Protein C Cofactor
|
|
Proc Cofactor Deficiency
|
Pccf Deficiency
|
|
Thrombophilia V
|
Thrombophilia, Susceptibility To, Due To Factor V Leiden
|
|
Thrombophilia Due To Factor V Leiden
|
Thrombophilia 2 Due To Activated Protein C Resistance
|
|
Thrombophilia, Susceptibility To, Due To Activated Protein C Resistance
|
|
|
| Glanzmann Thrombasthenia 1 |
|
Glanzmann Thrombasthenia
|
Thrombasthenia Of Glanzmann And Naegeli
|
|
Glanzmann'S Thrombasthenia
|
Bdplt2
|
|
Platelet Glycoprotein Iib-Iiia Deficiency
|
Deficiency Of Platelet Fibrinogen Receptor
|
|
GT1
|
Gt
|
|
Platelet Fibrinogen Receptor Deficiency
|
Glycoprotein Complex Iib-Iiia Deficiency
|
|
Deficiency Of Glycoprotein Complex Iib-Iiia
|
Glycoprotein Iib/Iiia Defect
|
|
Glanzmann Thrombasthenia, Type A
|
Thrombasthenia
|
|
Bleeding Disorder, Platelet-Type, 2
|
Gp Iib-Iiia Complex Deficiency
|
|
Deficiency Of Gp Iib-Iiia Complex
|
Platelet-Type Bleeding Disorder 2
|
|
Thrombocytasthenia
|
Deficiency Of Gp 2b 3a Complex
|
|
Diacyclothrombopathia 2b 3a
|
Glanzmann Thrombasthenia Type A
|
|
Platelet Fibrinogen Receptor, Deficiency Of
|
Platelet Glycoprotein 2b 3a Deficiency
|
|
Glanzmann Disease
|
Glanzmann-Naegeli Disorder
|
|
Hereditary Hemorrhagic Thrombasthenia
|
Hereditary Thrombasthenia
|
|
Bleeding Disorder Platelet-Type 2
|
|
|
| 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 Disorder Of Glycosylation, Type Ia |
|
CDG1A
|
Cdg Ia
|
|
Phosphomannomutase 2 Deficiency
|
Jaeken Syndrome
|
|
Pmm2-Congenital Disorder Of Glycosylation
|
Congenital Disorder Of Glycosylation Type Ia
|
|
Cdgia
|
Congenital Disorder Of Glycosylation Ia
|
|
Congenital Disorder Of Glycosylation 1a
|
Carbohydrate-Deficient Glycoprotein Syndrome Type Ia
|
|
Cdgs1a
|
Pmm2-Cdg
|
|
Cdg-Ia
|
Congenital Disorder Of Glycosylation Type 1a
|
|
Carbohydrate-Deficient Glycoprotein Syndrome, Type Ia, Formerly
|
Pmm Deficiency
|
|
Cdg Syndrome Type Ia
|
Carbohydrate Deficient Glycoprotein Syndrome Type Ia
|
|
Cdg Syndrome Type 1a
|
Jaeken'S Syndrome
|
|
Pmm2 Deficiency
|
Glycosylation, Congenital Disorder Of, Type Ia
|
|
|
| Retinal Artery Occlusion |
|
Retina Artery Narrowing
|
Retinal Artery Spasm
|
|
Spasm Of Ophthalmic Artery
|
Retinal Spasm
|
|
Vasospasm Of Retina
|
|
|
| Intracranial Hypertension |
|
Raised Intracranial Pressure
|
|
|
| Brachydactyly, Type D |
|
Brachydactyly Type D
|
BDD
|
|
Stub Thumb
|
Brachydactyly D
|
|
|
| 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
|
|
|
| Dilated Cardiomyopathy 1t |
|
Cmd1t
|
Cardiomyopathy, Dilated, 1t
|
|
|
| Thrombophilia Due To Thrombin Defect |
|
Venous Thromboembolism
|
Venous Thrombosis
|
|
Thrombophilia Due To Factor 2 Defect
|
Thromboembolism
|
|
THPH1
|
Thromboembolism, Susceptibility To
|
|
Venous Thromboembolism, Susceptibility To
|
Venous Thrombosis, Protection Against
|
|
Prothrombin-Related Thrombophilia
|
Hyperprothrombinemia
|
|
Venous Thrombosis, Susceptibility To
|
Thrombophilia 1 Due To Thrombin Defect
|
|
F2-Related Thrombophilia
|
Factor Ii-Related Thrombophilia
|
|
Prothrombin 20210g>A Thrombophilia
|
Prothrombin G20210a Thrombophilia
|
|
Prothrombin Thrombophilia
|
|
|
| Coumarin Resistance |
|
Warfarin Resistance
|
Warfarin Sensitivity
|
|
Coumadin Sensitivity
|
Warfarin Response
|
|
Poor Metabolism Of Coumarin
|
Coumarin, Poor Metabolism Of
|
|
CMRES
|
|
|
| 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
|
|
|
| Nephrotic Syndrome |
|
Finnish Congenital Nephrotic Syndrome
|
Ns - [Nephrotic Syndrome]
|
|
Nephrosis Syndrome
|
Nephrosis Nos
|
|
Glomerular Lesion Nephrosis
|
|
|
| Ornithine Transcarbamylase Deficiency, Hyperammonemia Due To |
|
Ornithine Carbamoyltransferase Deficiency
|
Ornithine Transcarbamylase Deficiency
|
|
Otc Deficiency
|
Ornithine Carbamoyltransferase Deficiency Disease
|
|
OTCD
|
Deficiency Of Citrulline Phosphorylase
|
|
Oct Deficiency
|
Hyperammonemia Due To Ornithine Carbamoyltransferase Deficiency
|
|
Deficiency, Ornithine Carbamoyltransferase
|
|
|
| Vitamin K Deficiency Bleeding |
|
Vitamin K Deficiency
|
Deficiency Of Vitamin K
|
|
Vitamin K
|
Vitamin K Deficiency Hemorrhagic Disease
|
|
|
| Prothrombin Deficiency |
|
Factor Ii Deficiency
|
Hypoprothrombinemia
|
|
Dysprothrombinemia
|
Deficiency, Prothrombin
|
|
Inherited Factor Ii Deficiency
|
Hereditary Factor Ii Deficiency Disease
|
|
|
| Acquired Immunodeficiency Syndrome |
|
Acquired Immune Deficiency Syndrome
|
AIDS
|
|
Acquired Immune Deficiency
|
Acquired Immunodeficiency
|
|
Acquired Immunodeficiency Due To Protein Loss
|
|
|
| Factor Xiii Deficiency |
|
Hereditary Factor Xiii Deficiency Disease
|
Deficiency, Laki-Lorand Factor
|
|
Congenital Factor Xiii Deficiency
|
Fibrin Stabilizing Factor Deficiency
|
|
Deficiency, Factor Xiii
|
Factor Xiii Deficiency Disease
|
|
Deficiency Of Factor Xiii
|
Fibrin-Stabilizing Factor Deficiency
|
|
Factor Xiii Deficiency, Congenital
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| Compartment Syndrome |
|
Compartment Syndromes
|
Compartmental Syndrome
|
|
|
| Tyrosinemia, Type I |
|
Tyrosinemia Type I
|
Hepatorenal Tyrosinemia
|
|
Fumarylacetoacetase Deficiency
|
Fah Deficiency
|
|
TYRSN1
|
Fumarylacetoacetate Hydrolase Deficiency
|
|
Tyrosinemia Type 1
|
Tyrosinemia 1
|
|
Fumarylacetoacetase
|
|
|
| Ulcer Of Lower Limbs |
|
Ulcer Of Ankle
|
Ulcer Of Calf
|
|
Ulcer Of Heel And Midfoot
|
Ulcer Of Thigh
|
|
Ulcer Of Lower Limb
|
|
|
| Gaucher'S Disease |
|
Gaucher Disease
|
Kerasin Thesaurismosis
|
|
Glucocerebrosidase Deficiency
|
Glucosylceramidase Deficiency
|
|
Cerebroside Lipidosis Syndrome
|
Acid Beta-Glucosidase Deficiency
|
|
Glucosylceramide Beta-Glucosidase Deficiency
|
Acute Cerebral Gaucher Disease
|
|
Gaucher Splenomegaly
|
Glucocerebrosidosis
|
|
Glucosyl Cerebroside Lipidosis
|
Kerasin Lipoidosis
|
|
Lipoid Histiocytosis
|
Glocucerebrosidase Deficiency
|
|
Sphingolipidosis 1
|
Gaucher Syndrome
|
|
Gauchers Disease
|
Gd
|
|
Glucosylceramide Lipidosis
|
Kerasin Histiocytosis
|
|
Gaucher Disease, Type 1
|
Gaucher Disease, Type 2
|
|
|
| Mucopolysaccharidosis, Type Ii |
|
Hunter Syndrome
|
Iduronate 2-Sulfatase Deficiency
|
|
Mucopolysaccharidosis Ii
|
Mps Ii
|
|
Mucopolysaccharidosis Type Ii
|
MPS2
|
|
Sulfoiduronate Sulfatase Deficiency
|
Mucopolysaccharidosis, Mps-Ii
|
|
Ids Deficiency
|
Sids Deficiency
|
|
I2s Deficiency
|
Mucopolysaccharidosis Type 2
|
|
Mucopolysaccharidosis Type 2, Severe Form
|
Deficiency Of Iduronate-2-Sulphatase
|
|
Hunter'S Syndrome
|
Mps Ii - Hunter Syndrome
|
|
Iduronate-2-Sulfatase Deficiency
|
Attenuated Mps
|
|
Mps 2
|
Severe Mps Ii
|
|
Mpsii
|
Mucopolysaccharidosis Type 2, Attenuated Form
|
|
Hunter Syndrome Type B
|
Iduronate 2-Sulfatase Deficiency Type B
|
|
Mps2b
|
Mpsiib
|
|
Mucopolysaccharidosis Type 2b
|
Mucopolysaccharidosis Type Ii, Attenuated Form
|
|
Mucopolysaccharidosis Type Iib
|
Hunter Syndrome Type A
|
|
Iduronate 2-Sulfatase Deficiency Type A
|
Mps2a
|
|
Mpsiia
|
Mucopolysaccharidosis Type 2a
|
|
Mucopolysaccharidosis Type Ii, Severe Form
|
Mucopolysaccharidosis Type Iia
|
|
Mucopolysaccharidosis 2
|
Hunters Syndrome
|
|
Iduronate 2-Sulphatase Deficiency
|
Iduronate Sulfatase Deficiency
|
|
Iduronate Sulphatase Deficiency
|
Sulfo-Iduronate Sulfatase Deficiency
|
|
Sulfoiduronidate Sulfatase Deficiency
|
Sulpho-Iduronate Sulphatase Deficiency
|
|
Sulphoiduronidate Sulphatase Deficiency
|
Mps2 - [Mucopolysaccharidosis 2]
|
|
|
| Bilirubin Metabolic Disorder |
|
Hyperbilirubinemia
|
Hereditary Hyperbilirubinemia
|
|
Hyperbilirubinemia, Hereditary
|
Hyperbilirubinaemia
|
|
|
| Adenosine Deaminase Deficiency |
|
Ada Deficiency
|
Ada-Scid
|
|
Severe Combined Immunodeficiency Due To Adenosine Deaminase Deficiency
|
Adenosine Deaminase Deficient Severe Combined Immunodeficiency
|
|
Scid Due To Ada Deficiency
|
Severe Combined Immunodeficiency Due To Ada Deficiency
|
|
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due To Adenosine Deaminase Deficiency
|
Ada
|
|
Scid Due To Adenosine Deaminase Deficiency
|
|
|
| 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
|
|
|
| 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
|
|
|
| Crigler-Najjar Syndrome, Type I |
|
Crigler-Najjar Syndrome
|
Crigler-Najjar Syndrome Type 1
|
|
Bilirubin Udp Glucuronyl Transferase Deficiency
|
Crigler Najjar Syndrome
|
|
Crigler Najjar Syndrome, Type 1
|
Bilirubin Uridinediphosphate Glucuronosyltransferase Deficiency
|
|
Bilirubin-Ugt Deficiency
|
Hyperbilirubinemia, Crigler-Najjar Type I
|
|
Hblrcn1
|
Familial Nonhemolytic Unconjugated Hyperbilirubinemia
|
|
Hereditary Unconjugated Hyperbilirubinemia
|
Bilirubin Uridinediphosphate Glucuronosyltransferase Deficiency Type 1
|
|
Bilirubin-Ugt Deficiency Type 1
|
Crigler-Najjar Syndrome 1
|
|
CN1
|
Cn-I
|
|
Crigler-Najjar Syndrome Type I
|
Hereditary Unconjugated Hyperbilirubinaemia
|
|
Ugt Deficiency
|
Bilirubin Glucuronosyltransferase Deficiency
|
|
Crigler-Najjar Disease Or Syndrome
|
Deficiency Of Glucuronosyltransferase
|
|
Glucuronyl Transferase Deficiency
|
Glucuronyltransferase Deficiency
|
|
Udp Glucuronyl Transferase Deficiency
|
Cns - [Crigler-Najjar Syndrome]
|
|
Congenital Familial Nonhemolytic Jaundice
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Stroke, Ischemic |
|
Cerebral Infarction
|
Stroke
|
|
Ischemic Stroke
|
Cerebrovascular Accident
|
|
Cerebral Infarction, Susceptibility To
|
Stroke, Ischemic, Susceptibility To
|
|
Cerebral Infarct
|
Ischemic Stroke, Susceptibility To
|
|
Stroke, Susceptibility To
|
Cva - Cerebral Infarction
|
|
ISCHSTR
|
Ischemic Cerebrovascular Accident
|
|
|
| Leber Plus Disease |
|
Leber Congenital Amaurosis
|
Lca
|
|
Leber'S Amaurosis
|
Leber'S Disease
|
|
Amaurosis Congenita Of Leber
|
Amaurosis Congenita Of Leber, Type 1
|
|
Lhon Plus Disease
|
Congenital Absence Of The Rods And Cones
|
|
Congenital Retinal Blindness
|
Crb
|
|
Congenital Amaurosis Of Retinal Origin
|
Leber'S Congenital Amaurosis
|
|
Leber Congenital Amaurosis 1
|
Leber'S Congenital Tapetoretinal Degeneration
|
|
Leber'S Congenital Tapetoretinal Dysplasia
|
Lca1
|
|
Leber Congenital Amaurosis Type 1
|
Retinal Blindness, Congenital
|
|
Amaurosis, Leber Congenital
|
Dysgenesis Neuroepithelialis Retinae
|
|
Hereditary Epithelial Dysplasia Of Retina
|
Hereditary Retinal Aplasia
|
|
Heredoretinopathia Congenitalis
|
Leber Abiotrophy
|
|
Leber Congenital Tapetoretinal Degeneration
|
Lebers Congenital Amaurosis
|
|
Optic Atrophy, Hereditary, Leber
|
|
|
| Type 2 Diabetes Mellitus |
|
Insulin Resistance
|
NIDDM
|
|
Type 2 Diabetes
|
Diabetes Mellitus, Non-Insulin-Dependent
|
|
T2D
|
Noninsulin-Dependent Diabetes Mellitus
|
|
Diabetes Mellitus, Type Ii
|
Maturity-Onset Diabetes
|
|
Insulin Resistance, Severe, Digenic
|
Diabetes Mellitus, Type 2
|
|
Diabetes Mellitus, Noninsulin-Dependent
|
Diabetes Mellitus, Noninsulin-Dependent, Association With
|
|
Diabetes Mellitus, Noninsulin-Dependent, Late Onset
|
Hypertension, Insulin Resistance-Related, Susceptibility To
|
|
Insulin Resistance, Susceptibility To
|
Non-Insulin-Dependent Diabetes Mellitus
|
|
Type Ii Diabetes Mellitus
|
Adult-Onset Diabetes Mellitus
|
|
Maturity-Onset Diabetes Mellitus
|
Diabetes Mellitus Type 2
|
|
Type Ii Diabetes
|
Type 2 Diabetes Mellitus, Susceptibility To
|
|
Diabetes, Type 2
|
Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To
|
|
Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 2, Susceptibility To
|
|
Diabetes Mellitus, Noninsulin-Dependent, 2
|
Diabetes Mellitus, Type Ii, Susceptibility To
|
|
Hypertension, Insulin Resistance-Related
|
Adult-Onset Diabetes
|
|
Aodm
|
Diabetes Mellitus, Adult-Onset
|
|
Diabetes Mellitus Type Ii
|
Diabetes Mellitus Type 2, Susceptibility To
|
|
Diabetes, Type Ii, Susceptibility To
|
Diabetes Type 2
|
|
Diabetes Mellitus
|
Adult Onset Diabetes
|
|
Maturity Onset Diabetes
|
Nonketotic Diabetes
|
|
Non-Insulin Dependent Diabetes Mellitus
|
T2dm - [Type 2 Diabetes Mellitus]
|
|
Niddm - [Non Insulin Dependent Diabetes Mellitus]
|
Dm2
|
|
Dm Type Ii
|
Diabetic Type 2
|
|
Insulin Requiring Type 2 Diabetes
|
Noninsulin Dependent Diabetes
|
|
Non-Insulin-Dependent Diabetes Mellitus Without Complications
|
Diabetes Due To Insulin Secretory Defect
|
|
Diabetes Mellitus Due To Insulin Secretory Defect
|
Non-Insulin-Dependent Diabetes Of The Young
|
|
Senile Diabetes
|
Nonketotic Hyperglycaemia
|
|
Stable Diabetes
|
|
|
| Fanconi Anemia, Complementation Group A |
|
Fanconi Anemia
|
Fanconi Pancytopenia
|
|
Fanconi Anemia Complementation Group A
|
FANCA
|
|
Fa
|
Fanconi Panmyelopathy
|
|
Fanconi'S Anemia
|
Fanconi Anaemia
|
|
Fanconi'S Anaemia
|
Fanconi Hypoplastic Anemia
|
|
Estren-Dameshek Variant Of Fanconi Anemia
|
Estren-Dameshek Variant Of Fanconi Pancytopenia
|
|
Fanconi Anemia Estren-Dameshek Variant
|
Fanconis Anemia
|
|
|
| Fundus Dystrophy |
|
Retinal Dystrophy
|
Retinal Dystrophies
|
|
Dystrophy, Retinal
|
|
|
