| Diseases |
Alias |
|
| Homocystinuria Due To Deficiency Of N -Methylenetetrahydrofolate Reductase Activity |
|
Homocystinuria Due To Mthfr Deficiency
|
Methylenetetrahydrofolate Reductase Deficiency
|
|
Mthfr Deficiency
|
Homocystinuria Due To Methylene Tetrahydrofolate Reductase Deficiency
|
|
5,10 Alpha Methylenetetrahydro-Folate Reductase Deficiency
|
5,10-Alpha-Methylenetetrahydro-Folate Reductase Deficiency
|
|
Homocysteinemia Due To Methylenetetrahydro-Folate Reductase Deficiency
|
Homocysteinuria Due To Methylenetetrahydro-Folate Reductase Deficiency
|
|
Methylenetetrahydro-Folate Reductase Deficiency
|
Methylene Tetrahydrofolate Reductase Deficiency
|
|
MTHFRD
|
5,10-Methylenetetrahydrofolate Reductase Deficiency
|
|
|
| Neural Tube Defects, Folate-Sensitive |
|
Neural Tube Defects, Folate-Sensitive, Susceptibility To
|
Neural Tube Defect, Folate-Sensitive
|
|
NTDFS
|
Ntd, Folate-Sensitive
|
|
Neural Tube Defects, Susceptibility To
|
Neural Tube Defects
|
|
|
| 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
|
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Spasticity |
|
|
| West Syndrome |
|
Infantile Spasms
|
Infantile Spasms Syndrome
|
|
Infantile Spasm
|
X-Linked Infantile Spasm Syndrome
|
|
X-Linked Infantile Spasms
|
Epileptic Encephalopathy, Early Infantile, 1
|
|
Is
|
Tonic Spasms With Clustering, Arrest Of Psychomotor Development And Hypsarrhythmia On Eeg
|
|
West'S Syndrome
|
Spasms, Infantile
|
|
Is -[Infantile Spasm]
|
Salaam Spasm
|
|
Salaam Tic
|
|
|
| Neural Tube Defects |
|
Spina Bifida
|
Neural Tube Defect
|
|
NTD
|
Neural Tube Defects, Susceptibility To
|
|
Spinal Dysraphism
|
Spina Bifida, Susceptibility To
|
|
Rachischisis
|
Cleft Spine
|
|
Open Spine
|
Hydrocele Spinalis
|
|
Neural Tube Defect Nos
|
Sb - [Spina Bifida]
|
|
Spinal Hernia Nos
|
Spinal Fissure Nos
|
|
|
| Homocysteinemia |
|
|
| Myelomeningocele |
|
|
| Isolated Exencephaly |
|
|
| Isolated Anencephaly |
|
|
| Vascular Disease |
|
Vascular Diseases
|
Aneurysm
|
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
| Homocystinuria |
|
Cystathionine Beta Synthase Deficiency
|
Homocysteinemia
|
|
Cbs Deficiency
|
Cystathionine Synthase Deficiency
|
|
Cystathionine Beta-Synthase Deficiency Disease
|
|
|
| Retinal Vein Occlusion |
|
Occlusion, Of Retinal Vein
|
|
|
| Upper Thoracic Spina Bifida Cystica |
|
|
| Cervicothoracic Spina Bifida Cystica |
|
|
| Cervical Spina Bifida Cystica |
|
|
| Lumbosacral Spina Bifida Cystica |
|
|
| Thoracolumbosacral Spina Bifida Cystica |
|
|
| Total Spina Bifida Cystica |
|
|
| Upper Thoracic Spina Bifida Aperta |
|
|
| Thoracolumbosacral Spina Bifida Aperta |
|
|
| Lumbosacral Spina Bifida Aperta |
|
|
| Cervical Spina Bifida Aperta |
|
Spina Bifida Aperta Of Cervical Spine
|
|
|
| Cervicothoracic Spina Bifida Aperta |
|
|
| Total Spina Bifida Aperta |
|
|
| Central Retinal Vein Occlusion |
|
|
| Hyperhomocysteinemia |
|
|
| Spina Bifida Occulta |
|
|
| Vitamin B12 Deficiency |
|
Cobalamin Deficiency
|
Hypocobalaminemia
|
|
Vitamin B 12 Deficiency
|
Cyanocobalamin Deficiency
|
|
Deficiency Of Vitamin B12
|
|
|
| Nonarteritic Anterior Ischemic Optic Neuropathy |
|
Anterior Ischemic Optic Neuropathy
|
Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To
|
|
NAION
|
Non-Arteritic Anterior Ischemic Optic Neuropathy
|
|
Ischemic Optic Neuropathy
|
Aion
|
|
Optic Neuropathy, Ischemic
|
Naion, Susceptibility To
|
|
Optic Neuropathy, Anterior Ischemic
|
Optic Neuropathy, Anterior Ischemic, Susceptibility To
|
|
Non-Arteritic Anterior Ischaemic Optic Neuropathy
|
Nonarteritic Anterior Ischaemic Optic Neuropathy
|
|
Neuropathy, Optic, Ischemic, Nonarteritic Anterior, Susceptibility To
|
Ion - [Ischemic Optic Neuropathy]
|
|
Neuropathic Ischaemia Of N.Opticus
|
Ischaemic Neuropathy Of Optic Nerve
|
|
|
| Anencephaly |
|
Aprosencephaly
|
Anencephalus
|
|
Congenital Absence Of Brain
|
Absence Of A Large Part Of The Brain And The Skull
|
|
Anencephalia
|
Anencephalic Monster
|
|
Brain Absence
|
Brain Agenesis
|
|
Brain Aplasia
|
Absent Brain
|
|
Anencephalic
|
Congenital Absence Of Cerebrum
|
|
Congenital Hemicrania
|
Incomplete Anencephaly
|
|
|
| Retinal Artery Occlusion |
|
Retina Artery Narrowing
|
Retinal Artery Spasm
|
|
Spasm Of Ophthalmic Artery
|
Retinal Spasm
|
|
Vasospasm Of Retina
|
|
|
| Riboflavin Deficiency |
|
Ariboflavinosis
|
Maternal Riboflavin Deficiency
|
|
RBFVD
|
Vitamin B2 Deficiency
|
|
Hyporiboflavinosis
|
|
|
| Protein S Deficiency |
|
Protein S Deficiency Disease
|
Hereditary Thrombophilia Due To Protein S Deficiency
|
|
|
| Placental Abruption |
|
Abruptio Placentae
|
Abruptio Placenta
|
|
Abortion, Threatened
|
Threatened Miscarriage
|
|
Haemorrhage Specified As Due To Threatened Abortion
|
Spontaneous Threatened Abortion
|
|
|
| Protein C Deficiency |
|
Hereditary Thrombophilia Due To Protein C Deficiency
|
Proc Deficiency
|
|
Congenital Thrombotic Disease, Due To Protein C Deficiency
|
|
|
| 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
|
|
|
| Gastroschisis |
|
Laparoschisis
|
Congenital Fissure Of The Abdominal Cavity
|
|
Abdominal Wall Defect
|
Abdominal Hernia
|
|
Hernia, Abdominal
|
Omphalocele
|
|
Abnormality Of The Abdominal Wall
|
Congenital Omphalocele
|
|
Coeloschisis
|
Coelioschisis
|
|
Celoschisis
|
Congenital Para-Umbilical Hernia
|
|
|
| Cerebrovascular Disease |
|
Cerebrovascular Disorder
|
Cerebrovascular Accident
|
|
Cerebrovascular Disorders
|
Cva
|
|
Stroke
|
|
|
| Hemifacial Spasm |
|
Facial Hemispasm
|
Focal Myoclonus Of Face
|
|
|
| Thrombophilia |
|
|
| Placenta Disease |
|
Placenta Diseases
|
Placenta Disorder
|
|
Pregnancy Complications
|
Placenta Disorders
|
|
|
| Nondisjunction |
|
Mosaicism, Chromosomal
|
Mixoploidy, Familial
|
|
|
| Thrombophlebitis |
|
Phlebitis And Thrombophlebitis Of Superficial Vessels Of Lower Extremities
|
Superficial Thrombophlebitis Of Leg
|
|
Thrombophlebitis Of A Superficial Leg Vein
|
Thrombophlebitis Of Superficial Veins Of Lower Extremity
|
|
|
| Eclampsia |
|
Eclampsia In Puerperium
|
Postpartum Eclampsia
|
|
Eclampsia, Postpartum
|
Puerperal Eclampsia
|
|
|
| Childhood Acute Lymphocytic Leukemia |
|
Childhood Acute Lymphoblastic Leukemia
|
Childhood All
|
|
Pediatric Acute Lymphoblastic Leukemia
|
Lymphoblastic Leukemia Acute Childhood
|
|
|
| Pulmonary Embolism |
|
Pulmonary Artery Embolism
|
Pulmonary Embolus
|
|
Pulmonary Emboli
|
|
|
| Budd-Chiari Syndrome |
|
Hepatic Vein Thrombosis
|
Chiari Syndrome
|
|
BDCHS
|
Membranous Obstruction Of The Inferior Vena Cava
|
|
Budd-Chiari Syndrome, Somatic
|
Movc
|
|
Budd-Chiari Syndrome, Susceptibility To, Somatic
|
Budd-Chiari Syndrome, Susceptibility To
|
|
Membranous Obstruction Of Inferior Vena Cava
|
Hepatic Vein Block
|
|
Obstruction Of Hepatic Veins
|
Hepatic Vein Obstruction
|
|
Hepatic Venous Block
|
|
|
| Antiphospholipid Syndrome |
|
Antiphospholipid Antibody Syndrome
|
Hughes Syndrome
|
|
Familial Antiphospholipid Syndrome
|
Aps
|
|
Lupus Anticoagulant, Familial
|
Anti-Phospholipid Syndrome
|
|
Apls
|
Classic Apls
|
|
Classic Antiphospholipid Syndrome
|
Acromegaloid Facial Appearance Syndrome
|
|
Anticardiolipin Syndrome
|
|
|
| Antithrombin Iii Deficiency |
|
Hereditary Antithrombin Deficiency
|
Congenital Antithrombin Iii Deficiency
|
|
Hereditary Thrombophilia Due To Congenital Antithrombin Deficiency
|
AT3D
|
|
Thrombophilia Due To Antithrombin Iii Deficiency
|
Thph7
|
|
Hereditary Thrombophilia Due To Congenital Antithrombin 3 Deficiency
|
Thrombophilia 7 Due To Antithrombin Iii Deficiency
|
|
At Iii Deficiency
|
Congenital At-Iii Deficiency
|
|
Inherited Antithrombin Deficiency
|
Antithrombin 3 Deficiency
|
|
Antithrombin Deficiency
|
Antithrombin-Iii Deficiency
|
|
At-Iii Deficiency
|
Thrombophilia Due To Antithrombin-Iii Deficiency
|
|
|
| Encephalomalacia |
|
|
| 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
|
|
|
| Amino Acid Metabolic Disorder |
|
Amino Acid Metabolism, Inborn Errors
|
Inborn Errors Of Amino Acid Metabolism
|
|
Disorder Of Amino Acid Metabolism
|
Amino Acid Metabolism Disorders
|
|
|
| Hellp Syndrome |
|
Hemolysis, Elevated Liver Enzymes, Lowered Platelets
|
Hemolysis, Elevated Liver Enzymes, Low Platelets In Pregnancy
|
|
Hemolysis-Elevated Liver Enzymes-Low Platelets Syndrome
|
Hellp - [Syndrome Of Haemolysis, Elevated Liver Enzymes And Low Platelet]
|
|
Haemolysis-Elevated Liver Enzymes-Low Platelet Count Syndrome
|
|
|
| Portal Vein Thrombosis |
|
Phlebitis Of Portal Vein
|
Deep Vein Thrombosis Of Portal Vein
|
|
Portal Thrombosis
|
Pvt - [Portal Vein Thrombosis]
|
|
Portal Venous Thrombosis
|
Portal Venous Embolism
|
|
Portal Venous Obstruction
|
Portal Venous Block
|
|
Portal Vein Embolism
|
Portal Vein Block
|
|
Portal Obstruction
|
Portal Embolism
|
|
Portal Block
|
Hepatic Portal Vein Obstruction
|
|
Occlusion Of Hepatic Portal Vein
|
Portal Vein Obstruction
|
|
|
| Amaurosis Fugax |
|
Transient Monocular Blindness
|
Momentary Blindness
|
|
Af - [Amaurosis Fugax]
|
Transient Vision Loss, Spontaneous
|
|
Amaurosis Fugax, Course Of Resolution Unspecified
|
|
|
| Adult Acute Lymphocytic Leukemia |
|
Adult Acute Lymphoid Leukemia
|
Adult All
|
|
|
| Migraine Without Aura |
|
Common Migraine
|
Migraine With Or Without Aura, Susceptibility To
|
|
Migraine Without Aura, Susceptibility To
|
Acute Migraine Without Aura
|
|
|
| Glycine N-Methyltransferase Deficiency |
|
GNMT DEFICIENCY
|
Hypermethioninemia Due To Glycine N-Methyltransferase Deficiency
|
|
Hypermethioninemia Due To Gnmt Deficiency
|
Hypermethioninemia
|
|
Hepatic Methionine Adenosyltransferase Deficiency
|
|
|
| Thrombosis |
|
Thrombosis Of Blood Vessel
|
|
|
| Cleft Lip |
|
Cheiloschisis
|
Labium Leporinum
|
|
Cleft Lip, Unilateral, Complete
|
Complete Unilateral Cleft Lip
|
|
Hare Lip
|
Congenital Fissure Of Lip
|
|
Isolated Cleft Lip
|
Cleft Lip Without Cleft Palate
|
|
Cleft Lip Without Cleft Palate, Unilateral
|
Isolated Cleft Lip, Unilateral
|
|
Cleft Lip Without Cleft Palate, Bilateral
|
Isolated Cleft Lip, Bilateral
|
|
|
| Migraine With Aura |
|
Classic Migraine
|
Migraine With Typical Aura
|
|
Migraine Accompagnée
|
Complicated Migraine
|
|
Classical Migraine
|
Acute Migraine With Aura
|
|
|
| Pre-Eclampsia |
|
Preeclampsia
|
Gestational Hypertension
|
|
Hypertension Induced By Pregnancy
|
Pre-Eclamptic Toxaemia
|
|
Pregnancy Associated Hypertension
|
Proteinuric Hypertension Of Pregnancy
|
|
Hypertension, Pregnancy-Induced, Susceptibility To
|
Preeclampsia/Eclampsia
|
|
Pregnancy Toxemia
|
Toxaemia Of Pregnancy
|
|
Gestational Proteinuric Hypertension
|
Pregnancy-Induced Hypertension
|
|
Toxemia Of Pregnancy
|
Preeclampsia, Susceptibility To
|
|
Transient Hypertension Of Pregnancy
|
Gestational [Pregnancy-Induced] Hypertension Without Significant Proteinuria
|
|
Gestational Hypertension Nos
|
Mild Proteinuric Hypertension Of Pregnancy
|
|
Pih - [Pregnancy-Induced Hypertension]
|
Pregnancy-Induced Hypertension Nos
|
|
Gestational [Pregnancy-Induced] Hypertension With Significant Proteinuria
|
Pe - [Pre-Eclampsia]
|
|
Pre-Eclampsia Nos
|
Pre-Eclamptic Nos
|
|
Pregnancy Pre-Eclampsia
|
Puerperal Pre-Eclampsia
|
|
Pre-Eclampsia Toxaemia
|
Toxaemia In Pregnancy
|
|
Pet - [Pre-Eclamptic Toxaemia]
|
Maternal Toxaemia
|
|
|
| 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
|
|
|
| Mucositis |
|
Inflammatory Disease Of Mucous Membrane
|
Gastrointestinal Mucositis
|
|
|
| Cervical Intraepithelial Neoplasia |
|
|
| Vascular Dementia |
|
Dementia, Vascular
|
Multi Infarct Dementia
|
|
Multifocal Dementia
|
Dementia Vascular
|
|
Vascular Dementia, Susceptibility To
|
Dementia, Multi-Infarct
|
|
Multi-Infarct Dementia
|
|
|
| Exfoliation Syndrome |
|
Pseudoexfoliation Glaucoma
|
Pseudoexfoliation Syndrome
|
|
Exfoliation Syndrome, Susceptibility To
|
XFS
|
|
Exfoliation Glaucoma
|
Xfg
|
|
Pseudoexfoliation Of The Lens
|
Pexg
|
|
Pexs
|
Exfoliative Syndrome
|
|
Glaucoma Capsulare
|
Pex
|
|
Pseudo-Exfoliation Syndrome
|
|
|
| Multiple Chemical Sensitivity |
|
Environmental Illness
|
20th Century Disease
|
|
Chemical Aids
|
Idiopathic Environmental Illness
|
|
Total Allergy Syndrome
|
|
|
| Intracranial Thrombosis |
|
Cerebral Thrombosis
|
Thrombosis Of Cerebral Veins
|
|
Cerebral Arterial Thrombosis
|
|
|
| Bipolar Disorder |
|
Bipolar Depression
|
Manic Disorder
|
|
Depression, Bipolar
|
Bipolar Disorder Manic Phase
|
|
Depressive-Manic Psych.
|
Manic Bipolar Affective Disorder
|
|
Manic Bipolar I Disorder
|
Manic Depression
|
|
Manic Depressive Disorder
|
Mixed Bipolar Disorder
|
|
Bipolar Affective Disorder
|
Bipolar Affective Psychosis
|
|
Bipolar Spectrum Disorder
|
Manic Depressive Illness
|
|
Depression Bipolar
|
Bipolar Disorder, Mixed
|
|
Major Affective Disorder
|
Major Affective Disorder 1
|
|
Major Affective Disorder 2
|
|
|
| Carotid Stenosis |
|
Carotid Artery Stenosis
|
Stenosis, Carotid Artery
|
|
|
| Venous Insufficiency |
|
Peripheral Venous Insufficiency
|
|
|
| Osteonecrosis |
|
Bone Necrosis
|
Avascular Necrosis Of Bone
|
|
Aseptic Necrosis
|
Necrosis Of Bone Nos
|
|
Aseptic Osteonecrosis
|
Aseptic Necrosis Of Bone, Site Unspecified
|
|
Aseptic Or Avascular Bone Necrosis
|
Aseptic Necrosis Of Bone
|
|
Necrotic Bone
|
Necrotizing Bone
|
|
Spontaneous Osteonecrosis
|
Osteoradionecrosis
|
|
|
| Nutritional Deficiency Disease |
|
Malnutrition
|
Nutritional Disorder
|
|
Nutritional Deficiency
|
Nutrition
|
|
Deficiency Diseases
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
|
Nutrition Disorders
|
|
|
| Vitamin Metabolic Disorder |
|
|
| Down Syndrome |
|
Trisomy 21
|
Complete Trisomy 21 Syndrome
|
|
Down'S Syndrome
|
Trisomy 21 Syndrome
|
|
Down'S Syndrome - Trisomy 21
|
Downs Syndrome
|
|
G Trisomy
|
47,Xx,+21
|
|
47,Xy,+21
|
Trisomy G
|
|
Down Syndrome, Susceptibility To
|
Chromosome 21 Trisomy
|
|
Trisomy 21 Nos
|
Abnormal Autosomes 21
|
|
|
| Peripheral Vascular Disease |
|
Peripheral Arterial Disease
|
Arterial Occlusive Disease
|
|
Arterial Occlusive Diseases
|
Pad
|
|
Peripheral Vascular Diseases
|
Peripheral Occlusive Disease
|
|
Peripheral Arterial Diseases
|
Helicobacter Infections
|
|
|
| Varicose Veins |
|
Varices
|
Varix
|
|
Venous Ectasia
|
Venous Varices
|
|
Varicosity
|
|
|
| Megaloblastic Anemia |
|
Imerslund-Grasbeck Syndrome
|
Igs
|
|
Defect Of Enterocyte Intrinsic Factor Receptor
|
Enterocyte Cobalamin Malabsorption
|
|
Familial Megaloblastic Anemia
|
Megaloblastic Anemia 1
|
|
Selective Cobalamin Malabsorption With Proteinuria
|
Imerslund-Gräsbeck Syndrome
|
|
Anemia, Megaloblastic
|
Grasbeck-Imerslund Syndrome
|
|
Megaloblastic Anaemia
|
Mga1 Norwegian Type
|
|
Recessive Hereditary Megaloblastic Anaemia 1
|
Recessive Hereditary Megaloblastic Anemia 1
|
|
Rh-Mga1
|
Gräsbeck-Imerslund Disease
|
|
Pernicious Anemia, Juvenile, Due To Selective Intestinal Malabsorption Of Vitamin B12, With Proteinuria
|
Juvenile Pernicious Anemia With Proteinuria Due To Selective Intestinal Malabsorption Of Vitamin B12
|
|
Anemia Megaloblastic
|
Megaloblastic Anemia Due To Inborn Errors Of Metabolism
|
|
3-@Methylglutaconic Aciduria, Type I
|
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| Lateral Sinus Thrombosis |
|
Thrombosis Of Lateral Venous Sinus
|
Thrombosis Transverse Sinus
|
|
|
| Methylmalonic Acidemia |
|
Methylmalonic Aciduria
|
Mma
|
|
Acidemia, Methylmalonic
|
Isolated Methylmalonic Acidemia
|
|
|
| Transient Cerebral Ischemia |
|
Transient Ischemic Attack
|
Transient Ischemic Attacks
|
|
Tia
|
Tia - Transient Ischaemic Attack
|
|
Transient Cerebral Ischaemia
|
Ischemic Attack, Transient
|
|
Intermittent Cerebral Ischemia
|
Tia - [Transient Ischaemic Attack]
|
|
Intermittent Cerebral Ischaemia
|
Transient Cerebral Ischaemic Attack, Unspecified, Course Of Resolution Unspecified
|
|
|
| Cleft Palate, Isolated |
|
Cleft Palate
|
Isolated Cleft Palate
|
|
CPI
|
Cp
|
|
Palatoschisis
|
Cleft Palate Isolated
|
|
Uranostaphyloschisis
|
Congenital Fissure Of Palate
|
|
Cleft Of Secondary Palate
|
|
|
| Psychotic Disorder |
|
Psychotic Disorders
|
Mental Or Behavioural Disorder
|
|
Psychotic
|
Mental Disorders
|
|
|
| Leukemia |
|
Leukemias
|
Leukaemia, Unspecified, Without Mention Of Remission
|
|
Aleukemic Leukaemia
|
Chronic Leukaemia
|
|
Subacute Leukaemia
|
Leukaemia Disorder
|
|
Leukaemia Nos
|
|
|
| Nephrosclerosis |
|
|
| Livedoid Vasculitis |
|
Livedoid Vasculopathy
|
Livedo Reticularis With Summer Ulcerations
|
|
Livedo Vasculitis
|
Livedo Reticularis With Winter Ulcerations
|
|
Segmental Hyalinizing Vasculopathy
|
Milian Atrophie Blanche
|
|
Segmental Hyalinizing Vasculitis
|
Livedo Reticularis With Summer Ulceration
|
|
|
| Myelitis |
|
Spinal Cord Inflammation Nos
|
Radiculomyelitis Nos
|
|
Myeloradiculitis
|
|
|
| Smallpox |
|
Variola
|
Ordinary Smallpox
|
|
Alastrim
|
Amaas
|
|
|
| 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
|
|
|
| Schizoaffective Disorder |
|
Schizo-Affective Psychosis
|
Schizo-Affective Type Schizophrenia
|
|
Schizoaffective Psychosis
|
Schizoaffective Schizophrenia
|
|
Schizophrenia, Schizo-Affective Type
|
Schizophreniform Psychosis, Affective Type
|
|
|
| Branch Retinal Artery Occlusion |
|
Retinal Artery Occlusion
|
Arterial Retinal Branch Occlusion
|
|
Retinal Arterial Branch Occlusion
|
|
|
| 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
|
|
|
| Male Infertility |
|
Infertility, Male
|
Infertility Male
|
|
Male Sterility
|
Absolute Infertility
|
|
|
| Intracranial Sinus Thrombosis |
|
Sinus Thrombosis, Intracranial
|
|
|
| Prothrombin Thrombophilia |
|
Prothrombin G20210a Thrombophilia
|
Hyperprothrombinemia
|
|
|
| Turner Syndrome |
|
Monosomy X
|
Gonadal Dysgenesis Turner Type
|
|
Ullrich-Turner Syndrome
|
Bonnevie-Ullrich Syndrome
|
|
Karyotype 45, X
|
Genital Dwarfism, Turner Type
|
|
Gonadal Dysgenesis
|
45,X
|
|
Turner'S Syndrome
|
Gonadal Dysgenesis - Turner
|
|
Monosomy X Syndrome
|
Xo Syndrome
|
|
Genital Dwarfism
|
45, X Syndrome
|
|
Bonnevie-Ulrich Syndrome
|
Chromosome X Monosomy X
|
|
Schereshevkii Turner Syndrome
|
Turner Varny Syndrome
|
|
Ts
|
45,X Syndrome
|
|
45,X/46,Xx Syndrome
|
Turners Syndrome
|
|
Gonadal Dysgenesis, 45,X
|
X0 Syndrome
|
|
|
| Retinal Vascular Occlusion |
|
Retinal Vasc. Occlusion
|
Occlusion Of Retinal Vessels
|
|
Retinal Obstruction
|
|
|
| Thrombasthenia |
|
|
| Pregnancy Loss, Recurrent 1 |
|
Pregnancy Loss, Recurrent, Susceptibility To, 1
|
Rpl
|
|
RPRGL1
|
Rprgl
|
|
Recurrent Miscarriage
|
Recurrent Spontaneous Abortion
|
|
Abortion, Spontaneous, Recurrent
|
Fetal Loss, Recurrent
|
|
Fetal Loss, Recurrent, Susceptibility To
|
Miscarriage, Recurrent
|
|
Embryonic Loss, Recurrent
|
Stillbirth, Recurrent
|
|
Pregnancy Loss, Recurrent, 1
|
Recurrent Embryonic Loss
|
|
Recurrent Fetal Loss
|
Recurrent Stillbirth
|
|
Spontaneous Recurrent Abortion
|
Miscarriage Recurrent
|
|
Pregnancy Loss, Recurrent, Susceptibility To, Type 1
|
Abortion, Habitual
|
|
|
| Clubfoot |
|
Congenital Talipes Equinovarus
|
Congenital Clubfoot
|
|
Congenital Equinovarus
|
Equinovarus Deformity Of Foot
|
|
Club Foot
|
|
|
| Hyperuricemia |
|
Blood Urate Raized
|
Uricacidemia
|
|
|
| Marfan Syndrome |
|
MFS
|
Mfs1
|
|
Marfan'S Syndrome
|
Marfan Syndrome Type 1
|
|
Marfan Syndrome, Type I
|
Mass Phenotype
|
|
Contractural Arachnodactyly
|
Mass Syndrome
|
|
Octd
|
Overlap Connective Tissue Disease
|
|
Marfanoid Hypermobility Syndrome
|
Marfan Disease
|
|
|
| Tetralogy Of Fallot |
|
TOF
|
Fallot Tetralogy
|
|
Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle
|
Tetrad Of Fallot
|
|
Fallot Tetrad
|
Fallot Disease
|
|
Fallot Complex
|
Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy
|
|
Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle
|
Interventricular Septal Defect, In Tetralogy Of Fallot
|
|
Ventricular Septal Defect With Obstructed Right Ventricular Outflow
|
Tof - [Tetralogy Of Fallot]
|
|
Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]
|
Pulmonary Atresia, Ventricular Septal Defect And Mapcas
|
|
Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]
|
|
|
| Central Nervous System Origin Vertigo |
|
Vertigo Of Central Origin
|
Vertigo
|
|
Central Vestibular Vertigo
|
|
|
| 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
|
|
|
| Migraine With Or Without Aura 1 |
|
Migraine
|
Migraine With Or Without Aura, Susceptibility To, 1
|
|
Migraine Disorder
|
Migraine Variant
|
|
Migraines
|
Migraine Disorders
|
|
Mgr1
|
Mgau
|
|
Ma
|
Migraine With Or Without Aura
|
|
Classic Migraine
|
Common Migraine
|
|
Disorder, Migraine
|
Headache Migraine
|
|
Headache Migrainous
|
Migraine Headache
|
|
Migraine Syndrome
|
Headache Including Migraine
|
|
Migraine, Susceptibility To
|
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Varicocele |
|
Scrotal Varices
|
Varicoceles
|
|
Varicocele Of Scrotum
|
Scrotal Varicocele
|
|
|
| Lipoprotein Quantitative Trait Locus |
|
Coronary Artery Disease
|
Coronary Artery Anomaly
|
|
Coronary Artery Disease, Susceptibility To
|
Myocardial Ischemia
|
|
Congenital Anomaly Of Coronary Artery
|
Coronary Arteriosclerosis
|
|
Coronary Disease
|
Coronary Heart Disease
|
|
Coronary Artery Disorder
|
LPAQTL
|
|
Lpa Deficiency, Congenital
|
Coronary Artery Abnormality
|
|
Coronary Artery Anomaly, Congenital
|
Chd
|
|
Coronary Syndrome
|
Congenital Malformations Of Coronary Vessels
|
|
Malformation Of Coronary Vessels
|
Congenital Coronary Artery Anomaly
|
|
Congenital Coronary Artery Deformity
|
Congenital Coronary Artery Disorder
|
|
Abnormal Coronary Artery
|
Congenital Coronary Artery Malposition
|
|
Congenital Coronary Disease
|
Congenital Anomaly Of Coronary Arteries
|
|
|
| Takayasu Arteritis |
|
Aortic Arch Syndrome
|
Pulseless Disease
|
|
Takayasu'S Arteritis
|
Idiopathic Aortitis
|
|
Young Female Arteritis
|
Aortic Arch Arteritis
|
|
Aortic Arches Defect
|
Aortic Arch Defects
|
|
Takayasu Disease
|
Aortic Arch Syndromes
|
|
Takayasu'S Disease
|
Ta
|
|
Obliterative Aortitis
|
Aortic Arch Giant-Cell Arteritis
|
|
Subclavian-Carotid Obstruction Syndrome
|
Idiopathic Medial Aortopathy And Arteriopathy
|
|
Takayasu Syndrome
|
Obliterative Brachiocephalic Arteritis Syndrome
|
|
Raeder-Harbitz Syndrome
|
Chronic Subclavian-Carotid Obstruction Syndrome
|
|
Giant-Cell Aortitis
|
Takayasu Aortitis
|
|
Nonspecific Aortoarteritis
|
Sclerosing Aortitis And Arteritis
|
|
Martorell 2 Syndrome
|
Young Female Aortic Arch Arteritis 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
|
|
|
| Pseudoxanthoma Elasticum |
|
PXE
|
Gronblad-Strandberg Syndrome
|
|
Pseudoxanthoma Elasticum, Modifier Of Severity Of
|
Gronblad-Strandberg-Touraine Syndrome
|
|
Gronblad Strandberg Syndrome
|
Groenblad-Strandberg Syndrome
|
|
Nevus Elasticus
|
Pxe - [Pseudoxanthoma Elasticum]
|
|
|
| Sagittal Sinus Thrombosis |
|
Thrombosis Of Superior Longitudinal Sinus
|
Thrombosis Of Superior Sagittal Sinus
|
|
Thrombosis Superior Sagittal Sinus
|
|
|
| Central Retinal Artery Occlusion |
|
|
| Microphthalmia, Isolated 5 |
|
Isolated Microphthalmia 5
|
MCOP5
|
|
Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen
|
Microphthalmia-Retinitis Pigmentosa-Foveoschisis-Optic Disc Drusen Syndrome
|
|
Posterior Microphthalmia With Retinitis Pigmentosa, Foveoschisis And Optic Disc Drusen
|
Nanophthalmos-Retinitis Pigmentosa-Foveoschisis-Optic Disc Drusen Syndrome
|
|
Microphthalmia, Isolated, 5
|
Microphthalmia Mfrp-Related
|
|
Posterior Microphthalmia With Retinitis Pigmentosa, Foveoschisis And Optic Disk Drusen
|
Microphthalmia, Isolated, Type 5
|
|
|
| Vein Disease |
|
|
| Mastoiditis |
|
|
| Atherosclerosis Susceptibility |
|
Atherosclerosis
|
Atherosclerosis, Susceptibility To
|
|
ATHS
|
Atherogenic Lipoprotein Phenotype
|
|
Alp
|
Arteriosclerosis
|
|
|
| Cerebral Palsy |
|
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
|
Palsy Cerebral
|
Palsy, Cerebral
|
|
Cerebral Palsy, Mixed
|
|
|
| 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
|
|
|
| Leukemia, Acute Lymphoblastic |
|
Acute Lymphoblastic Leukemia
|
ALL
|
|
Acute Lymphocytic Leukemia
|
Leukemia, Acute Lymphocytic, Susceptibility To, 1
|
|
Acute Lymphoblastic Leukaemia
|
Precursor Lymphoblastic Lymphoma/Leukemia
|
|
Precursor Lymphoid Neoplasm
|
Leukemia, Acute Lymphoblastic, Susceptibility To
|
|
B-Cell Acute Lymphoblastic Leukemia
|
Leukemia, Acute Lymphocytic 1
|
|
Acute Lymphocytic Leukaemia
|
Acute Lymphoblastic Leukemia/Lymphoma
|
|
All1
|
Childhood Acute Lymphoblastic Leukemia
|
|
Leukemia Acute Lymphoblastic 1
|
Leukemia Acute Lymphoblastic B-Hyperdiploid
|
|
Leukemia Acute Lymphocytic
|
Leukemia Acute Lymphocytic 1
|
|
Leukemia B-Cell Acute Lymphoblastic
|
Leukemia T-Cell Acute Lymphoblastic
|
|
Leukemia, Acute Lymphoblastic, 3
|
ALL3
|
|
Lymphoblastic Leukemia Acute
|
Leukemia, Acute, Lymphoblastic
|
|
Precursor Cell Lymphoblastic Leukemia Lymphoma
|
Leukemia, Lymphocytic, Acute, L1
|
|
Leukemia, Acute Lymphoblastic, Susceptibility To, 3
|
|
|
| Blood Protein Disease |
|
Blood Protein Disorders
|
Blood Protein Disorder
|
|
|
| Hydrocephalus |
|
Hydrocephalus, Nonsyndromic, Autosomal Recessive
|
Hydrocephalus, X-Linked
|
|
Hydrocephalus Adverse Event
|
Hydrocephaly Nos
|
|
|
| Diabetes Mellitus |
|
|
| 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
|
|
|
| Cardia Cancer |
|
Ca Cardia - Stomach
|
Malignant Neoplasm Of Cardia Of Stomach
|
|
|
| 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
|
|
|
| Glycogen Storage Disease |
|
Glycogenosis
|
Glycogenoses
|
|
Gsd
|
Storage Disease, Glycogen
|
|
Gsd - [Glycogen Storage Disease]
|
Glycogen Thesaurismosis
|
|
Diffuse Glycogenosis
|
Generalised Glycogen Storage Disease
|
|
Generalised Glycogenosis
|
Generalised Glycogen Storage Disease Of Infants
|
|
Glycogen Synthase Deficiency
|
|
|
| Rheumatoid Arthritis |
|
RA
|
Arthritis, Rheumatoid
|
|
Rheumatoid Arthritis, Susceptibility To
|
Arthritis Or Polyarthritis, Rheumatic
|
|
Atrophic Arthritis
|
Rheumatism Arthritis
|
|
Rheumatoid Polyarthritis
|
|
|
| Biotinidase Deficiency |
|
Late-Onset Multiple Carboxylase Deficiency
|
BTD DEFICIENCY
|
|
Multiple Carboxylase Deficiency, Late-Onset
|
Multiple Carboxylase Deficiency, Juvenile-Onset
|
|
Juvenile-Onset Multiple Carboxylase Deficiency
|
Biotin Deficiency
|
|
Late-Onset Biotin-Responsive Multiple Carboxylase Deficiency
|
Deficiency Of Biotinidase
|
|
Biot
|
Carboxylase Deficiency, Multiple, Late-Onset
|
|
Late-Onset Mcd
|
Mcd Juvenile Form
|
|
Biotin Deficiency Disease
|
|
|
| Meningocele |
|
Isolated Spina Bifida
|
Spina Bifida
|
|
Cleft Spine
|
Open Spine
|
|
Rachischisis
|
Spinal Dysraphism
|
|
Spinal Meningocele
|
Congenital Meningocele
|
|
|
| Tobacco Addiction |
|
Nicotine Dependence
|
Tobacco Addiction, Susceptibility To
|
|
Nicotine Addiction
|
Tobacco Use Disorder
|
|
Smoking Habit
|
Nicotine Dependence, Protection Against
|
|
Nicotine Addiction, Protection From
|
Cigarette Habituation
|
|
Cigarette Habituation, Susceptibility To
|
Smoking Habit, Susceptibility To
|
|
Nicotine Dependence, Susceptibility To
|
Nicotine Addiction, Susceptibility To
|
|
Addiction, Tobacco, Susceptibility To
|
Compulsive Tobacco User Syndrome
|
|
Tobacco Dependence
|
Tobacco Dependence Syndrome
|
|
Cigarette Addiction
|
Cigarette Dependence
|
|
Smoking Addiction
|
Smokers Syndrome
|
|
|
| Hypermethioninemia |
|
Hepatic Methionine Adenosyltransferase Deficiency
|
Deficiency Of Methionine Adenosyltransferase
|
|
Glycine N-Methyltransferase Deficiency
|
Met
|
|
S-Adenosylhomocysteine Hydrolase Deficiency
|
Gnmt Deficiency
|
|
Mat Deficiency
|
Methionine Adenosyltransferase Deficiency
|
|
Methioninemia
|
Deficiency Of Acetyl-Coa Acetyltransferase
|
|
|
| Choline Deficiency Disease |
|
|
| Physical Disorder |
|
|
| Intracranial Hypotension |
|
|
| Gastric Cancer |
|
Stomach Cancer
|
Gastric Carcinoma
|
|
Stomach Carcinoma
|
Gastric Cancer, Somatic
|
|
Gastric Neoplasm
|
Carcinoma Of Stomach
|
|
Stomach Neoplasms
|
Malignant Neoplasm Of Stomach
|
|
Gastric Cancer Risk After H. Pylori Infection
|
Cancer Of The Stomach
|
|
Adult Stomach Cancer
|
Adult Stomach Carcinoma
|
|
GASC
|
Gastric Cancer Intestinal
|
|
Gastric Cancers
|
Gastric Carcinomas
|
|
Cancer, Gastric
|
Stomach Neoplasm
|
|
Malignant Neoplasm Of Body Of Stomach
|
Malignant Tumor Of Lesser Curve Of Stomach
|
|
Gastrocarcinoma Of Unspecified Site
|
Leather Bottle Stomach
|
|
Carcinoma Of Fundus Of Stomach
|
Cancer Of Fundus Of Stomach
|
|
Primary Malignant Neoplasm Of Body Of Stomach
|
Cancer Of Body Of Stomach
|
|
Primary Malignant Neoplasm Of Pyloric Antrum
|
Pyloric Antrum Cancer
|
|
Malignant Tumour Of Stomach
|
|
|
| Cerebral Atherosclerosis |
|
Intracranial Arteriosclerosis
|
|
|
| Pulmonary Artery Disease |
|
Abnormality Of The Pulmonary Artery
|
|
|
| Methylmalonic Aciduria And Homocystinuria, Cblc Type |
|
MAHCC
|
Vitamin B12 Metabolic Defect With Combined Deficiency Of Methylmalonyl-Coa Mutase And Homocysteine:Methyltetrahydrofolate Methyltransferase
|
|
Methylmalonic Aciduria And Homocystinuria, Cblc Type, Digenic
|
Methylmalonic Aciduria And Homocystinuria Type Cblc
|
|
Cobalamin C Disease
|
Methylmalonic Acidemia With Homocystinuria Cblc
|
|
Methylmalonic Acidemia And Homocystinuria, Cblc Type
|
Methylmalonic Aciduria And Homocystinuria, Vitamin B12-Responsive
|
|
Cobalamin C Deficiency
|
Methylmalonic Acidemia With Homocystinuria, Type Cblc
|
|
Cblc Defect
|
Cobalamin C Defect
|
|
Combined Defect In Adenosylcobalamin And Methylcobalamin Synthesis, Type Cblc
|
Methylmalonic Aciduria With Homocystinuria, Type Cblc
|
|
Methylmalonic Acidemia And Homocystinuria Cblc Type
|
Methylmalonic Aciduria And Homocystinuria Vitamin B12-Responsive
|
|
Aciduria, Methylmalonic, And Homocystinuria, Cblc Type
|
Methylmalonic Acidemia With Homocystinuria
|
|
|
| Patent Foramen Ovale |
|
Atrial Septal Defect Within Oval Fossa
|
Foramen Ovale Patent
|
|
Ostium Secundum Atrial Septal Defect
|
Atrial Septal Defect, Ostium Secundum Type
|
|
Foramen Ovale, Patent
|
Defect, Patent Or Persistent, Ostium Secundum
|
|
Ostium Secundum Type Atrial Septal Defect
|
Persistent Ostium Secundum
|
|
Asd Ostium Secundum Type
|
Ostium Secundum Asd
|
|
Osasd
|
Asd, Ostium Secundum Type
|
|
Pfo - [Patent Foramen Ovale]
|
Open Foramen Ovale
|
|
Open Oval Foramen
|
Persistent Foramen Ovale
|
|
Secundum Atrial Septal Defect
|
|
|
| Type 1 Diabetes Mellitus |
|
Diabetes Mellitus, Insulin-Dependent
|
Diabetes Mellitus Type 1
|
|
IDDM
|
Type 1 Diabetes
|
|
Insulin-Dependent Diabetes Mellitus
|
T1D
|
|
Juvenile-Onset Diabetes
|
Jod
|
|
Diabetes Mellitus, Type 1
|
Diabetes Mellitus, Insulin-Dependent-1
|
|
Type I Diabetes Mellitus
|
Autoimmune Diabetes
|
|
Juvenile Diabetes
|
Juvenile-Onset Diabetes Mellitus
|
|
Diabetes, Insulin Dependent
|
Insulin-Dependent Diabetes Mellitus-1
|
|
Diabetes Mellitus Insulin-Dependent
|
Diabetes Autoimmune
|
|
Diabetes Mellitus, Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 1, Susceptibility To
|
|
Diabetes Type 1
|
Type I Diabetes
|
|
Diabetes, Autoimmune
|
T1dm - [Type 1 Diabetes Mellitus]
|
|
Iddm - [Insulin Dependent Diabetes Mellitus]
|
Type 1 Iddm
|
|
Juvenile Diabetes Mellitus Without Compications
|
Idiopathic Insulin-Dependent Diabetes Mellitus Without Complications
|
|
Juvenile-Onset Diabetes Mellitus Without Compications
|
Ketosis-Prone Diabetes Mellitus Without Compications
|
|
Juvenile-Onset-Type Diabetes Mellitus Without Compications
|
|
|
| Vertical Talus, Congenital |
|
Congenital Vertical Talus
|
CVT
|
|
Congenital Convex Pes Valgus
|
Rocker-Bottom Foot Deformity
|
|
Vertical Talus
|
Pes Valgus, Congenital Convex
|
|
Congenital Convex Foot
|
Congenital Rocker-Bottom Foot
|
|
Rocker Bottom Foot
|
Flatfoot
|
|
Rocker-Bottom Foot
|
Charcot-Marie-Tooth Disease, Foot Deformity Of
|
|
|
| Autoimmune Disease Of Cardiovascular System |
|
|
| Moyamoya Disease 1 |
|
Moyamoya Disease
|
Spontaneous Occlusion Of The Circle Of Willis
|
|
Mymy
|
Progressive Intracranial Arterial Occlusion
|
|
Moyamoya Syndrome
|
MYMY1
|
|
Cerebrovascular Moyamoya Disease
|
Moya-Moya Disease
|
|
Progressive Intracranial Occlusive Arteropathy
|
Idiopathic Moyamoya Disease
|
|
|
| Autism Spectrum Disorder |
|
Asd
|
Autism Spectrum Disorders
|
|
Autistic Continuum
|
Pervasive Developmental Disorder
|
|
Pervasive Development Disorder
|
Autistic Behavior
|
|
Autistic Disorder
|
Autistic
|
|
Autistic Disorder Of Childhood Onset
|
Infantile Autism
|
|
Childhood Autism
|
Kanner Syndrome
|
|
Pervasive Developmental Delay Nos
|
Pervasive Developmental Disorder, Not Otherwise Specified
|
|
|
| Methylmalonic Aciduria, Cbla Type |
|
Methylmalonic Acidemia Cbla Type
|
Methylmalonic Aciduria Cbla Type
|
|
Methylmalonic Acidemia, Cbla Type
|
Methylmalonic Aciduria, Vitamin B12-Responsive, Due To Defect In Synthesis Of Adenosylcobalamin, Cbla Type
|
|
Methylmalonic Aciduria, Vitamin B12-Responsive, Cbla Type
|
Methylmalonic Aciduria, Vitamin B12-Responsive Due To A Defect In Synthesis Of Adenosylcobalamin Cb1a Type
|
|
Vitamin B12-Responsive Methylmalonic Acidemia Type Cbla
|
Vitamin B12-Responsive Methylmalonic Aciduria Type Cbla
|
|
Methylmalonic Aciduria Type Cbla
|
MMAA
|
|
Methylmalonic Aciduria Type A
|
Vitamin B12 Responsive Methylmalonic Acidemia Type Cbl A
|
|
Vitamin B12 Responsive Methylmalonic Aciduria Type Cbl A
|
Aciduria, Methylmalonic, Cbla Type
|
|
Methylmalonic Aciduria Cbla Type
|
|
|
| Argininemia |
|
Hyperargininemia
|
Arginase Deficiency
|
|
Arg1 Deficiency
|
Arginase-1 Deficiency
|
|
Deficiency Of Canavanase
|
Arginase Deficiency Disease
|
|
ARGIN
|
|
|
| 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
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| Colorectal Cancer, Hereditary Nonpolyposis, Type 5 |
|
HNPCC5
|
Hereditary Nonpolyposis Colorectal Cancer Type 5
|
|
Hereditary Non-Polyposis Colorectal Cancer 5
|
Cancer, Colorectal, Nonpolyposis, Hereditary, Type 5
|
|
|
| Huntington Disease |
|
Huntington'S Disease
|
Huntington Chorea
|
|
Huntington'S Chorea
|
HD
|
|
Huntington Chronic Progressive Hereditary Chorea
|
Juvenile Huntington Disease
|
|
Chronic Progressive Chorea
|
Chronic Progressive Hereditary Chorea
|
|
Hc - [Huntington Chorea]
|
Hereditary Chorea
|
|
Progressive Hereditary Chorea
|
|
|
| Basal Cell Carcinoma |
|
Basal Cell Cancer
|
Basal Cell Neoplasm
|
|
Basal Cell Carcinoma Of Skin
|
Malignant Basal Cell Tumor
|
|
Basal Cell Tumor
|
Epithelioma Basal Cell
|
|
Malignant Basal Cell Neoplasm
|
Rodent Ulcer
|
|
Carcinoma Basal Cell
|
Neoplasms, Basal Cell
|
|
Basal Cell Carcinomas
|
Experimental Organism Basal Cell Carcinoma
|
|
Nodulo-Ulcerative Basal Cell Carcinoma
|
Basalioma
|
|
Basal Cell Epithelioma Of Skin
|
Bcc - [Basal Cell Carcinoma] Of Skin
|
|
Rodent Ulcer Of Skin
|
Rodent Ulcer Of Unspecified Site
|
|
Basal Cell Epithelioma Of Unspecified Site
|
|
|
| Atrial Heart Septal Defect |
|
Atrial Septal Defect
|
Atrial Septal Defects
|
|
Atrioseptal Defect
|
Auricular Septal Defect
|
|
Congenital Atrial Septal Defect
|
Interatrial Septal Defect
|
|
Interauricular Septal Defect
|
Heart Septal Defects, Atrial
|
|
Septal Defect, Atrial
|
|
|
| Myopia |
|
Near-Sightedness
|
Short-Sightedness
|
|
Nearsightedness
|
Nearsighted
|
|
Near Vision
|
Close Sighted
|
|
Myopic
|
Short-Sighted
|
|
Near Sighted
|
|
|
| Orofacial Cleft |
|
|
| Chromosomal Duplication Syndrome |
|
|
| Autism |
|
Autistic Disorder
|
Autism Susceptibility 1
|
|
Childhood Autism
|
Autistic Disorder Of Childhood Onset
|
|
Infantile Autism
|
Kanner'S Syndrome
|
|
Autistic
|
|
|
| Cataract |
|
Cataracts
|
Cat - [Cataract]
|
|
Cataract Form
|
Lens Opacity
|
|
Lens Opacities
|
|
|
| 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
|
|
|
| Colorectal Adenoma |
|
Colorectal Adenomas
|
Adenoma Of Large Intestine
|
|
|
| Inflammatory Bowel Disease |
|
Inflammatory Bowel Diseases
|
Bowel Disease, Inflammatory
|
|
|
| Breast Cancer |
|
Breast Carcinoma
|
Male Breast Cancer
|
|
Breast Cancer, Familial
|
Malignant Neoplasm Of Breast
|
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
|
Mammary Cancer
|
Mammary Tumor
|
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
|
Familial Breast Cancer
|
Cancer Of Breast
|
|
BC
|
Breast Cancer Familial
|
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
|
Breast Male Carcinoma
|
Breast Neoplasms
|
|
Breast Neoplasms, Male
|
Mammary Tumors
|
|
Mammary Carcinomas
|
Cancer, Breast
|
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
|
Carcinoma With Apocrine Differentiation
|
|
|
| Spermatogenic Failure |
|
Azoospermia
|
Spgf
|
|
Spermatogenic Failure, Susceptibility To
|
Absent Sperm
|
|
Aspermatogenesis
|
Infertility Due To Azoospermia
|
|
Hypospermatogenesis
|
Azoospermatism
|
|
|
| Methylmalonic Aciduria And Homocystinuria, Cblx Type |
|
Mental Retardation, X-Linked 3
|
Methylmalonic Acidemia With Homocystinuria, Type Cblx
|
|
MAHCX
|
Intellectual Developmental Disorder, X-Linked 3
|
|
Xlid3
|
Mrx3
|
|
Methylmalonic Acidemia And Homocysteinemia Cblx Type
|
Combined Defect In Adenosylcobalamin And Methylcobalamin Synthesis, Type Cblx
|
|
Methylmalonic Aciduria With Homocystinuria, Type Cblx
|
Methylmalonic Acidemia And Homocysteinemia, Cblx Type
|
|
Methylmalonic Aciduria And Homocysteinemia, Cblx Type
|
Methylmalonic Aciduria And Homocysteinemia , Cblx Type
|
|
Mental Retardation, X-Linked, Type 3
|
|
|
| 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
|
|
|
| Behcet Syndrome |
|
Behcet Disease
|
Behcet'S Syndrome
|
|
Behcet'S Disease
|
Behçet Disease
|
|
Bd
|
Adamantiades-Behcet Disease
|
|
Triple Symptom Complex
|
Behçet'S Disease
|
|
Behet'S Syndrome
|
Bd Syndrome
|
|
Behçet Syndrome
|
Behçet'S Syndrome
|
|
Behcet Triple Symptom Complex
|
Malignant Aphthosis
|
|
Old Silk Route Disease
|
Adamantiades-Behçet Disease
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Congenital Nervous System Abnormality |
|
Congenital Neurologic Anomaly
|
Congenital Nervous System Disorder
|
|
|
