疾病名称 |
别名 |
|
Aortic Aneurysm, Familial Thoracic 4 |
AAT4
|
Faa4
|
Aortic Aneurysm/Aortic Dissection And Patent Ductus Arteriosus
|
Familial Aortic Aneurysm 4
|
Non-Syndromic Thoracic Aortic Aneurysms And Dissection
|
Taad
|
Thoracic Aortic Aneurysms And Dissection
|
Thoracic Aortic Aneurysms And Dissections
|
Aneurysm, Aortic, Thoracic, Familial, Type 4
|
|
|
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 2 |
|
|
Visceral Myopathy 2 |
|
|
Aortic Aneurysm, Familial Thoracic 1 |
Thoracic Aortic Aneurysm
|
Annuloaortic Ectasia
|
Familial Thoracic Aortic Aneurysm And Aortic Dissection
|
Familial Aortic Dissection
|
Familial Taad
|
Familial Thoracic Aortic Aneurysm
|
Congenital Aneurysm Of Ascending Aorta
|
Familial Aortic Aneurysm
|
Familial Thoracic Aortic Aneurysm And Dissection
|
Aortic Aneurysm, Thoracic
|
AAT1
|
Faa1
|
Aortic Dissection, Familial
|
Aortic Aneurysm, Familial Thoracic
|
Aneurysm, Thoracic Aortic
|
Faa
|
Ftaad
|
Taa
|
Taad
|
Cystic Medial Necrosis Of Aorta
|
Familial Non-Syndromic Thoracic Aortic Aneurysm And Aortic Dissection
|
Aortic Aneurysm Thoracic
|
Familial Aortic Aneurysms
|
Aneurysm, Aortic, Thoracic, Familial, Type 1
|
Aneurysm Of Thoracic Aorta
|
Intrathoracic Aneurysm
|
Thoracic Aorta Aneurysm
|
Thoracic Aortic Aneurysm Without Rupture
|
Thoracic Aneurysm
|
Thorax Arterial Aneurysm
|
Thoracic Artery Aneurysm
|
Thoracic Arterial Aneurysm
|
Thorax Aneurysm
|
Thorax Aortic Aneurysm
|
Dissection Of Thoracic Aorta
|
|
|
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 1 |
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome
|
Berdon Syndrome
|
MMIHS
|
Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
|
Megacystis, Microcolon, Hypoperistalsis Syndrome
|
Visceral Myopathy
|
Mmih Syndrome
|
Megacystis-Microcolon-Intestinal Hypoperistalsis-Hydronephrosis Syndrome
|
MMIHS1
|
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome, Mmih
|
Mmhs
|
|
|
Acute Myelomonocytic Leukemia |
Acute Myeloid Leukemia With Abnormal Bone Marrow Eosinophils Inv(16)(P13q22) Or T(16
|
16)(P13
|
Q22)
|
Aml M4
|
Ammol
|
Acute Myeloblastic Leukemia Type 4
|
Aml With Abnormal Bone Marrow Eosinophils Inv(16)(P13q22) Or T(16
|
16)(P13
|
Q22)
|
Aml-M4
|
Aml With Inv(16)(P13.1q22) Or T(16
|
16)(P13.1
|
Q22)
|
Cbfb-Myh11
|
Leukemia Myelomonocytic Acute
|
Leukemia, Myelomonocytic, Acute
|
Acute Myelomonocytic Leukaemia Without Mention Of Remission
|
Myelomonocytic Leukaemia Nos
|
|
|
Microcolon |
|
|
Tricuspid Valve Insufficiency |
Tricuspid Regurgitation
|
Tricuspid Valve Regurgitation
|
Tricuspid Incompetence
|
Tr - [Tricuspid Regurgitation]
|
Tricuspid Valve Incompetency
|
Tricuspid Valve Annular Incompetency
|
|
|
Intestinal Pseudo-Obstruction |
Chronic Intestinal Pseudoobstruction
|
Chronic Intestinal Pseudo-Obstruction
|
Cipo
|
Neuronal Intestinal Dysplasia
|
Hollow Visceral Myopathy
|
Familial Visceral Neuropathy
|
Paralytic Ileus
|
Intestinal Pseudoobstruction
|
Chronic Idiopathic Intestinal Pseudo-Obstruction
|
Ciip
|
Congenital Short Bowel Syndrome
|
Enteric Neuropathy
|
Familial Visceral Myopathy
|
Ipo
|
Pseudo-Obstruction Of Intestine
|
Pseudointestinal Obstruction Syndrome
|
Pseudoobstructive Syndrome
|
Congenital Idiopathic Intestinal Pseudoobstruction
|
Visceral Myopathy, Familial
|
|
|
Mitral Valve Insufficiency |
Mitral Regurgitation
|
Congenital Insufficiency Of Mitral Valve
|
Congenital Mitral Insufficiency
|
Congenital Mitral Regurgitation
|
Mitral Valve Incompetence
|
Mitral Valve Regurgitation
|
Mr - [Mitral Regurgitation]
|
Mi - [Mitral Incompetence]
|
Mitral Valve Annular Incompetency
|
Congenital Mitral Valve Incompetence
|
Congenital Mitral Valve Insufficiency
|
Congenital Mitral Valve Regurgitation
|
Congenital Mitral Incompetence
|
|
|
Myeloid Leukemia |
Myeloid Leukaemia
|
Leukaemia Myelogenous
|
Leukemia Myelogenous
|
Myeloid Granulocytic Leukaemia
|
Myeloid Granulocytic Leukemia
|
Non-Lymphocytic Leukemia
|
Leukemia, Myeloid
|
Granulocytic Leukaemia
|
Myelogenous Leukaemia
|
Myeloid Leukaemia, Unspecified, Without Mention Of Remission
|
|
|
Aortic Aneurysm |
Aortic Rupture
|
Thoracoabdominal Aortic Aneurysm, Ruptured
|
Ruptured Aortic Aneurysm
|
Aortic Aneurysms
|
Aortic Aneurysm Without Mention Of Rupture Nos
|
Ruptured Abdominal Aortic Aneurysm
|
Aortic Aneurysm, Ruptured
|
Ruptured Thoracic Aortic Aneurysm
|
|
|
Intraductal Papilloma |
Papilloma, Intraductal
|
Ductal Papilloma
|
Papilloma Intraductal
|
|
|
Aortic Dissection |
|
|
Visceral Myopathy 1 |
Visceral Myopathy
|
Megaduodenum And/Or Megacystis
|
VSCM1
|
Pseudoobstruction, Idiopathic Intestinal
|
Vscm
|
Pseudoobstruction Idiopathic Intestinal
|
Visceral Myopathy Familial
|
Berdon Syndrome
|
Idiopathic Intestinal Pseudoobstruction
|
Infantile Visceral Myopathy
|
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome
|
Mmih
|
Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
|
Intestinal Pseudo-Obstruction
|
Visceral Neuropathy, Familial, Autosomal Dominant
|
|
|
Leukemia |
Leukemias
|
Leukaemia, Unspecified, Without Mention Of Remission
|
Aleukemic Leukaemia
|
Chronic Leukaemia
|
Subacute Leukaemia
|
Leukaemia Disorder
|
Leukaemia Nos
|
|
|
Myopia |
Near-Sightedness
|
Short-Sightedness
|
Nearsightedness
|
Nearsighted
|
Near Vision
|
Close Sighted
|
Myopic
|
Short-Sighted
|
Near Sighted
|
|
|
Pleomorphic Adenoma |
Mixed Tumor Of The Salivary Gland
|
Adenoma Pleomorphic
|
Adenoma, Pleomorphic
|
Mixed Salivary Gland Tumor
|
Mixed Tumor, Not Otherwise Specified
|
|
|
Ectopic Pregnancy |
Eccyesis
|
Pregnancy Ectopic
|
Pregnancy, Ectopic
|
Ectopic Pregnancies
|
Extrauterine Gestation Or Pregnancy
|
Extrauterine Pregnancy
|
Ep - [Ectopic Pregnancy]
|
Ectopic Mole
|
Aborted Ectopic Pregnancy
|
Ruptured Ectopic Pregnancy
|
|
|
Core Binding Factor Acute Myeloid Leukemia |
Cbf Acute Myeloid Leukemia
|
Cbf-Aml
|
Core-Binding Factor Aml
|
|
|
Aortic Valve Disease 1 |
Aortic Valve Disease
|
Bicuspid Aortic Valve
|
Aortic Valve Disorder
|
AOVD1
|
Bav
|
Bicuspid Aortic Valve Disease
|
Familial Bicuspid Aortic Valve
|
Aortic Valve Calcification
|
Aovd
|
Aortic Valve, Bicuspid
|
Aortic Valve, Calcification Of
|
Aortic Stenosis, Calcific
|
Familial Bav
|
Calcific Aortic Stenosis
|
Calcification Of Aortic Valve
|
Abnormality Of The Aortic Valve
|
Aortic Valve Disease, Type 1
|
Aortic Valve Disease 2
|
Bicommissural Aortic Valve
|
|
|
Adenoid Cystic Carcinoma |
Adenocystic Carcinoma
|
Cribriform Carcinoma
|
Cylindroma
|
Carcinoma Adenoid Cystic
|
Carcinoma, Adenoid Cystic
|
Adenoid Cystic Carcinoma Of Salivary Gland
|
Eccrine Dermal Cylindroma
|
Carcinoma, Cribriform
|
|
|
Gastrointestinal Stromal Tumor |
GIST
|
Gastrointestinal Stromal Tumors
|
Gastrointestinal Stromal Sarcoma
|
Gastrointestinal Stromal Tumor, Familial
|
Gant
|
Gastrointestinal Stromal Tumour
|
Stromal Tumor Of Gastrointestinal Tract
|
Stromal Tumour Of Gastrointestinal Tract
|
Gastrointestinal Stromal Neoplasm
|
Paraganglioma And Gastric Stromal Sarcoma
|
Plexosarcoma
|
|
|
Hydronephrosis |
Stricture Of Ureteropelvic Junction With Hydronephrosis
|
Hydronephrosis With Ureteral Stricture, Not Elsewhere Classified
|
|
|
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]
|
|
|
Myopathy |
Muscular Diseases
|
Myopathies
|
|
|
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
|
|
|
Loeys-Dietz Syndrome |
Loeys-Dietz Aortic Aneurysm Syndrome
|
Lds
|
Aortic Aneurysm Syndrome Due To Tgf-Beta Receptors Anomalies
|
Furlong Syndrome
|
|
|
Ehlers-Danlos Syndrome, Vascular Type |
Eds Iv
|
Eds4
|
Vascular Ehlers-Danlos Syndrome
|
Veds
|
Sack-Barabas Syndrome
|
EDSVASC
|
Ehlers-Danlos Syndrome, Type Iv, Autosomal Dominant
|
Vascular Type Ehlers-Danlos Syndrome
|
Arterial-Ecchymotic Eds
|
Ehlers-Danlos Syndrome Type 4
|
Vascular Eds
|
Ehlers-Danlos Syndrome, Type 4
|
Ehlers-Danlos Syndrome, Type Iv
|
Ehlers-Danlos Syndrome, Arterial Type
|
Ehlers-Danlos Syndrome, Ecchymotic Type
|
Ehlers-Danlos Syndrome, Sack-Barabas Type
|
Autosomal Dominant Type Iv Ehlers-Danlos Syndrome
|
Eds Type Iv
|
Eds Type 4
|
Ehlers Danlos Syndrome, Sack-Barabas Type
|
Ehlers Danlos Syndrome, Arterial Type
|
Ehlers Danlos Syndrome, Ecchymotic Type
|
Ehlers-Danlos Syndrome Type Iv
|
Ehlers-Danlos Syndrome 4
|
Ehlers-Danlos Syndrome Arterial Type
|
Ehlers-Danlos Syndrome Ecchymotic Type
|
Ehlers-Danlos Syndrome, Type 4 Variant
|
Ehlers-Danlos, Vascular Type Syndrome
|
|
|
Hypereosinophilic Syndrome |
Eosinophilia
|
HES
|
Eosinophilic Leukocytosis
|
Hypereosinophilic Syndrome, Idiopathic
|
Idiopathic Hypereosinophilic Syndrome
|
Disseminated Eosinophilic Collagen Disease
|
Eosinophilic Disorder
|
Disorders With Increased Eosinophil Counts
|
|
|
Arterial Tortuosity Syndrome |
Arterial Tortuosity
|
Ats
|
ATORS
|
Tortuosity, Arterial, Syndrome
|
|
|
Prune Belly Syndrome |
Eagle-Barrett Syndrome
|
Abdominal Muscle Deficiency Syndrome
|
PBS
|
Abdominal Muscles, Absence Of, With Urinary Tract Abnormality And Cryptorchidism
|
Egbrs
|
Eagle-Barret Syndrome
|
Urethral Obstruction Sequence
|
Obrinsky Syndrome
|
Triad Syndrome
|
Obrisnksy Syndrome
|
Euos
|
Early Urethral Obstruction Sequence
|
Renal Dysplasia Or Hydronephrosis, Oligohydramnios And Subsequent Lung Hypoplasia Due To Urethral Obstruction
|
Absence Of Abdominal Muscles With Urinary Tract Abnormality And Cryptorchidism
|
Abdomen Muscle Deficiency Syndrome
|
Abdomen Muscular Deficiency Syndrome
|
Abdominal Muscular Deficiency Syndrome
|
Abdominal Muscle Aplasia Syndrome
|
|
|
Breast Ductal Carcinoma |
Ductal Breast Carcinoma
|
Duct Carcinoma
|
Carcinoma, Ductal
|
Mammary Ductal Carcinoma
|
Ductal Carcinoma
|
|
|
Loeys-Dietz Syndrome 3 |
LDS3
|
Aneurysms-Osteoarthritis Syndrome
|
Loeys-Dietz Syndrome With Osteoarthritis
|
Aneurysm-Osteoarthritis Syndrome
|
Lds1c
|
Loeys-Dietz Syndrome, Type 3
|
Loeys-Dietz Syndrome, Type 1c, Formerly
|
Lds1c, Formerly
|
Loeys-Dietz Syndrome Type 1c
|
Loeys-Dietz Syndrome Type 3
|
Aneurysm - Osteoarthritis Syndrome
|
Loeys-Dietz Syndrome, Type 1c
|
Aos
|
Loeys-Dietz Syndrome 1c
|
|
|
Aortic Disease |
Aortic Diseases
|
Aortic Disorder
|
Disorder Of The Aorta
|
|
|
Childhood Acute Myeloid Leukemia |
Childhood Acute Myeloid Leukaemia
|
Paediatric Acute Myeloid Leukaemia
|
Pediatric Acute Myeloid Leukemia
|
|
|
Char Syndrome |
Patent Ductus Arteriosus With Facial Dysmorphism And Abnormal Fifth Digits
|
CHAR
|
|
|
Myeloid Leukemia Associated With Down Syndrome |
|
|
Supravalvular Aortic Stenosis |
SVAS
|
Supravalvar Aortic Stenosis
|
Supravalvar Aortic Stenosis, Eisenberg Type
|
Aortic Supravalvular Stenosis
|
Aortic Stenosis, Supravalvular
|
Supra-Valvular Aortic Stenosis
|
Stenosis, Aortic Supravalvular
|
Stenosis, Supravalvular Aortic
|
Supravalvular Stenosis, Aortic
|
Aortic Stenosis Supravalvular
|
|
|
Aortic Valve Insufficiency |
Aortic Regurgitation
|
Rheumatic Aortic Regurgitation
|
Aortic Insufficiency
|
Rheumatic Aortic Insufficiency
|
Rheumatic Aortic Valve Insufficiency
|
Aortic Incompetence
|
Corrigan'S Disease
|
Rheumatic Aortic Valve Regurgitation
|
Aortic Valve Incompetency
|
Ai - [Aortic Incompetence]
|
Incompetent Aortic Valve
|
Ar - [Aortic Regurgitation]
|
Calcific Aortic Valve Regurgitation
|
Myxomatous Aortic Valve Regurgitation
|
Annular Incompetency Of Aortic Valve
|
Austin Flint Murmur
|
Flint Murmur
|
Rheumatic Aortic Incompetence
|
Rheumatic Ai - [Aortic Insufficiency]
|
|
|
Childhood Leukemia |
|
|
Urofacial Syndrome 1 |
Urofacial Syndrome
|
Ochoa Syndrome
|
Hydronephrosis With Peculiar Facial Expression
|
Ufs
|
Inverted Smile And Occult Neuropathic Bladder
|
Partial Facial Palsy With Urinary Abnormalities
|
UFS1
|
Urofacial Ochoa'S Syndrome
|
Urofacial Syndrome Type 1
|
Facial Palsy, Partial, With Urinary Abnormalities
|
Hydronephrosis-Inverted Smile
|
Inverted Smile-Neurogenic Bladder
|
Hydronephrosis-Inverted Smile Syndrome
|
Inverted Smile-Neurogenic Bladder Syndrome
|
Partial Facial Palsy Partial With Urinary Abnormalities
|
Urologic Diseases
|
|
|
Loeys-Dietz Syndrome 4 |
LDS4
|
Aneurysm, Aortic And Cerebral, With Arterial Tortuosity And Skeletal Manifestations
|
Loeys-Dietz Syndrome Type 4
|
Aortic And Cerebral Aneurysm With Arterial Tortuosity And Skeletal Manifestations
|
Loeys-Dietz Syndrome, Type 4
|
|
|
Nystagmus 3, Congenital, Autosomal Dominant |
NYS3
|
Congenital Nystagmus 3
|
Autosomal Dominant Congenital Nystagmus 3
|
|
|
Aortic Aneurysm, Familial Abdominal, 1 |
Abdominal Aortic Aneurysm
|
Aortic Aneurysm, Familial Abdominal 1
|
Aneurysm, Abdominal Aortic
|
AAA
|
Aortic Aneurysm, Abdominal
|
AAA1
|
Aortic Aneurysm, Familial Abdominal
|
Aortic Aneurysm Abdominal
|
Abdominal Aortic Aneurysms
|
Abdominal Aortic Aneurysm Without Mention Of Perforation Or Rupture
|
Abdomen Aneurysm
|
Abdominal Aorta Aneurysm
|
Aneurysm Of Abdominal Aorta
|
Aortic Abdomen Aneurysm
|
Aaa - [Abdominal Aortic Aneurysm]
|
Abdominal Aneurysm
|
Abdominal Aorta Aneurysm Rupture
|
Abdominal Aorta Aneurysm Ruptured
|
Abdominal Aortic Aneurysm Which Has Ruptured
|
Ruptured Aaa
|
Abdomen Aorta Aneurysm Ruptured
|
Abdomen Aorta Rupture
|
Abdomen Aortic Aneurysm Rupture
|
Abdomen Aneurysm Rupture
|
Abdomen Aortic Aneurysm Ruptured
|
Abdomen Aortic Rupture
|
Abdominal Aorta Rupture
|
Abdominal Aortic Rupture
|
Rupture Abdomen Aorta Aneurysm
|
Rupture Abdominal Aortic Aneurysm
|
Ruptured Abdomen Aneurysm
|
Ruptured Abdomen Aorta
|
Ruptured Abdomen Aortic
|
Ruptured Abdominal Aneurysm
|
Ruptured Abdominal Aorta
|
Ruptured Abdominal Aortic
|
Ruptured Aorta Abdominalis Aneurysm
|
False Abdomen Aorta Aneurysm Ruptured
|
False Abdominal Aortic Aneurysm Ruptured
|
False Abdominal Aorta Aneurysm Ruptured
|
False Abdomen Aortic Aneurysm Ruptured
|
|
|
Ectodermal Dysplasia 14, Hair/Tooth Type With Or Without Hypohidrosis |
ECTD14
|
Ectodermal Dysplasia 14
|
Ectn14
|
|
|
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
|
|
|
Vulvar Leiomyoma |
|
|
Orthostatic Intolerance |
Mitral Valve Prolapse
|
Neurocirculatory Asthenia
|
Mitral Valve Prolapse Syndrome
|
Irritable Heart
|
Systolic Click-Murmur Syndrome
|
Soldiers Heart
|
Cardiovascular Malfunction Arising From Mental Factors
|
Cardiovascular Neurosis
|
Da Costa'S Syndrome
|
Krishaber'S Disease
|
Barlow'S Syndrome
|
Floppy Mitral Valve
|
Mitral Leaflet Syndrome
|
Myxomatous Mitral Valve Prolapse
|
Postural Orthostatic Tachycardia Syndrome Due To Net Deficiency
|
Familial Orthostatic Tachycardia Due To Norepinephrine Transporter Deficiency
|
Orthostatic Intolerance Due To Net Deficiency
|
Pots Due To Net Deficiency
|
OI
|
Intolerance, Orthostatic
|
Mitral Valve Prolapse, Familial, X-Linked
|
Ballooning Mitral Valve
|
Barlow Syndrome
|
Flail Mitral Leaflet
|
Myxomatous Mitral Valve
|
Mitral Valve Prolapse-Click Syndrome
|
Prolapsing Mitral Valve Leaflet Syndrome
|
Billowing Mitral Valve Leaflet
|
Posterior Mitral Leaflet Deformity
|
Ballooning Posterior Leaflet Syndrome
|
Blue Valve Syndrome
|
Floppy Mitral Valve Syndrome
|
Mitral Valvular Prolapse
|
Systolic Click Syndrome
|
|
|
Ehlers-Danlos Syndrome |
Eds
|
Cutis Hyperelastica
|
Elastic Skin
|
Ehlers-Danlos Syndromes
|
Ed Syndrome
|
Ehlers Danlos Syndrome
|
Ehlers Danlos Disease
|
Eds - [Ehlers-Danlos Syndrome]
|
|
|
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
|
|
|
Leukemia, Acute Myeloid |
Acute Myeloid Leukemia
|
Leukemia, Acute Myelogenous
|
Acute Myelogenous Leukemia
|
AML
|
Leukemia, Acute Myeloid, Susceptibility To
|
Acute Myeloblastic Leukemia
|
Leukemia, Acute Myeloid, Reduced Survival In, Somatic
|
Acute Myeloid Leukaemia
|
Leukemia, Myelocytic, Acute
|
Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome
|
Secondary Aml
|
Acute Myelocytic Leukemia
|
Acute Myeloid Leukemia, Somatic
|
Leukemia, Acute Myeloid, Somatic
|
Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic
|
Acute Myeloblastic Leukaemia
|
Acute Myelogenous Leukaemia
|
Aml - Acute Myeloid Leukemia
|
Acute Myeloid Leukemia With Cebpa Somatic Mutations
|
Aml With Cebpa Somatic Mutations
|
Inherited Acute Myeloid Leukemia
|
Familial Aml
|
Inherited Aml
|
Pure Familial Aml
|
Pure Familial Acute Myeloid Leukemia
|
Secondary Acute Myeloid Leukemia
|
Therapy-Related Aml And Myelodysplastic Syndrome
|
Acute Myeloid Leukemia, Secondary
|
Acute Non-Lymphoblastic Leukemia
|
Acute Non-Lymphocytic Leukemia
|
Acute Biphenotypic Leukemia
|
Acute Undifferentiated Leukemia
|
Acute Myeloblastic Leukaemia With Multilineage Dysplasia
|
Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission
|
Acute Myeloid Leukaemia With Myelodysplasia-Related Features
|
|
|
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
|
|
|
Acute Promyelocytic Leukemia |
Leukemia, Acute Promyelocytic
|
Acute Myeloblastic Leukemia Type 3
|
Aml M3
|
APL
|
Leukemia, Acute Promyelocytic, Somatic
|
Aml With T(15
|
17)(Q22
|
Q12)
|
(Pml/Raralpha) And Variants
|
Apml
|
Acute Myeloblastic Leukemia 3
|
Acute Myeloid Leukemia With T(15
|
17)(Q22
|
Q12)
|
(Pml/Raralpha) And Variants
|
Acute Myeloblastic Leukaemia Type 3
|
Acute Myeloid Leukaemia M3
|
Acute Myeloid Leukemia M3
|
Acute Promyelocytic Leukaemia
|
M3 Anll
|
Myeloid Leukemia, Acute, M3
|
Leukemia Promyelocytic Acute
|
Leukemia, Promyelocytic, Acute
|
Leukemia, Acute, Promyelocytic
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 |
Asymmetric Septal Hypertrophy
|
Familial Hypertrophic Cardiomyopathy
|
Hypertrophic Cardiomyopathy 1
|
CMH1
|
Hypertrophic Cardiomyopathy 19
|
CMH
|
Ventricular Hypertrophy, Hereditary
|
Ash
|
Hypertrophic Subaortic Stenosis, Idiopathic
|
Cardiomyopathy, Familial Hypertrophic
|
Cardiomyopathy, Hypertrophic, 1, Digenic
|
Cardiomyopathy, Familial Hypertrophic 1
|
Hcm
|
Hereditary Ventricular Hypertrophy
|
Idiopathic Hypertrophic Subaortic Stenosis
|
Hypertrophic Cardiomyopathy
|
Cardiomyopathy, Hypertrophic, Familial
|
Cardiomyopathy, Hypertrophic, 1
|
Familial Asymmetric Septal Hypertrophy
|
Heritable Hypertrophic Cardiomyopathy
|
Fhc
|
Cardiomyopathy, Hypertrophic, Familial, Type 1
|
|
|
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]
|
|
|
Williams-Beuren Syndrome |
Williams Syndrome
|
WBS
|
Wms
|
Deletion 7q11.23
|
Monosomy 7q11.23
|
Chromosome 7q11.23 Deletion Syndrome, 1.5- To 1.8-Mb
|
Fanconi Schlesinger Syndrome
|
Beuren Syndrome
|
Elfin Facies Syndrome
|
Elfin Facies With Hypercalcemia
|
Hypercalcemia-Supravalvar Aortic Stenosis
|
Ws
|
|
|
Rasopathy |
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
|
Hypertrophic Cardiomyopathy |
Hypertrophic Obstructive Cardiomyopathy
|
Cardiomyopathy, Hypertrophic
|
Cardiomyopathy Hypertrophic Obstructive
|
Cardiomyopathy, Hypertrophic, Familial
|
Idiopathic Myocardial Hypertrophy
|
Idiopathic Hypertrophic Cardiomyopathy
|
Obstructive Idiopathic Hypertrophic Cardiomyopathy
|
Obstructive Cardiomyopathy
|
Idiopathic Hypertrophic Subaortic Stenosis
|
Muscular Subaortic Stenosis
|
Hypertrophic Obstructive Subaortic Stenosis
|
|
|
Dilated Cardiomyopathy |
Familial Dilated Cardiomyopathy
|
Primary Dilated Cardiomyopathy
|
Idiopathic Dilated Cardiomyopathy
|
Congestive Cardiomyopathy
|
Idiopathic Dilation Cardiomyopathy
|
Primary Familial Dilated Cardiomyopathy
|
Cardiomyopathy, Dilated
|
DCM
|
Cardiomyopathy, Familial Dilated
|
Dilated Cardiomyopathy, Familial
|
Hypokinetic Dilated Cardiomyopathy, Familial
|
Familial Idiopathic Cardiomyopathy
|
Fdc
|
Cardiomyopathy, Familial Idiopathic
|
Idiopathic Cardiomegaly
|
Dilated Congestive Cardiomyopathy
|
Chronic Dilated Cardiomyopathy
|
Ccm - [Congestive Cardiomyopathy]
|
Cocm - [Congestive Cardiomyopathy]
|
Dcm - [Dilated Cardiomyopathy]
|
Dilated-Hypokinetic Cardiomyopathy
|
Congestive Idiopathic Cardiomyopathy
|
Primary Idiopathic Dilated Cardiomyopathy
|
|
|