| 疾病名称 |
别名 |
|
| Cantu Syndrome |
|
Hypertrichotic Osteochondrodysplasia
|
Hypertrichotic Osteochondrodysplasia Cantu Type
|
|
Cantú Syndrome
|
Craniofaciocardioskeletal Syndrome
|
|
Hypertrichosis-Osteochondrodysplasia-Cardiomegaly Syndrome
|
Congenital Hypertrichosis-Acromegaloid Facial Features Spectrum
|
|
Congenital Hypertrichosis-Coarse Facial Features Spectrum
|
HTOCD
|
|
Osteochondrodysplasia, Hypertrichotic
|
|
|
| Atrial Fibrillation, Familial, 12 |
|
ATFB12
|
Fibrillation, Atrial, Familial, Type 12
|
|
|
| Cardiomyopathy, Dilated, 1o |
|
Dilated Cardiomyopathy 1o
|
CMD1O
|
|
Dilated Cardiomyopathy With Ventricular Tachycardia
|
Cardiomyopathy, Dilated, With Ventricular Tachycardia
|
|
Cardiomyopathy, Dilated 1o
|
Cardiomyopathy, Dilated, Type 1o
|
|
|
| Intellectual Disability And Myopathy Syndrome |
|
|
| Epicanthus |
|
|
| Hypermobile Ehlers-Danlos Syndrome |
|
Heds
|
Ehlers-Danlos Syndrome Type 3
|
|
Ehlers-Danlos Syndrome Hypermobility Type
|
Hypermobile Eds
|
|
Joint Hypermobility
|
Benign Joint Hypermobility Syndrome
|
|
Eds Hypermobility Type
|
Eds Type Iii
|
|
Ehlers-Danlos Syndrome Type Iii
|
Joint Hypermobility Syndrome
|
|
Eds3
|
Ehlers-Danlos Syndrome, Hypermobility Type
|
|
Eds Iii
|
Eds-Ht
|
|
|
| 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
|
|
|
| Fanconi Anemia, Complementation Group C |
|
Fanconi Anemia Complementation Group C
|
FANCC
|
|
Facc
|
Fac
|
|
Fa3
|
Fanconi Pancytopenia Type 3
|
|
Fanconi Pancytopenia, Type 3
|
Faces Syndrome
|
|
Facial Features , Anorexia, Cachexia, Eye And Skin Anomalies
|
Friedman-Goodman Syndrome
|
|
Abnormality Of The Face
|
|
|
| Familial Isolated Dilated Cardiomyopathy |
|
Familial Or Idiopathic Dilated Cardiomyopathy
|
|
|
| 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
|
|
|
| Kleefstra Syndrome 1 |
|
9q Subtelomeric Deletion Syndrome
|
KLEFS1
|
|
Chromosome 9q34.3 Deletion Syndrome
|
9q- Syndrome
|
|
9q34 Deletion Syndrome
|
Kleefstra Syndrome Due To 9q34 Microdeletion
|
|
Kleefstra Syndrome
|
9q-Syndrome
|
|
9qstds
|
Kleefstra Syndrome Due To 9q Subtelomeric Deletion
|
|
Kleefstra Syndrome Due To Del(9)(Q34)
|
Kleefstra Syndrome Due To Monosomy 9q34
|
|
Chromosome 9q Subtelomeric Deletion Syndrome
|
Kleefstra Syndrome, Type 1
|
|
|
| Hypertrichosis |
|
|
| Brugada Syndrome |
|
Sudden Unexpected Nocturnal Death Syndrome
|
Sudden Unexplained Nocturnal Death Syndrome
|
|
Bangungut
|
Brugada Type Idiopathic Ventricular Fibrillation
|
|
Pokkuri Death Syndrome
|
Sunds
|
|
Idiopathic Ventricular Fibrillation, Brugada Type
|
Sudden Unexplained Death
|
|
Dream Disease
|
Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome
|
|
Sudden Unexplained Death Syndrome
|
Suds
|
|
Sunds - [Sudden Unexplained Nocturnal Death Syndrome]
|
|
|
| Wolff-Parkinson-White Syndrome |
|
Wolff-Parkinson-White Pattern
|
Wpw Syndrome
|
|
Anomalous Atrioventricular Excitation
|
Anomalous A-V Excitation
|
|
Ventricular Pre-Excitation With Arrhythmia
|
WPWS
|
|
Ventricular Familial Preexcitation Syndrome
|
Preexcitation Syndrome
|
|
Ventricular Preexcitation
|
Wpw - [Wolff-Parkinson- White] Syndrome
|
|
Pre-Excitation Syndrome
|
|
|
| Familial Atrial Fibrillation |
|
Atrial Fibrillation, Familial
|
Atfb
|
|
Atrial Fibrillation Autosomal Dominant
|
Autosomal Dominant Atrial Fibrillation
|
|
Auricular Fibrillation
|
Atrial Fibrillation
|
|
Atrial Fibrillation, Familial, 1
|
|
|
| Atrial Fibrillation |
|
A-Fib
|
Fibrillation, Atrial
|
|
Af - [Atrial Fibrillation]
|
Rapid Atrial Fibrillation
|
|
A Fib - [Atrial Fibrillation]
|
|
|
| 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]
|
|
|
| Arteriolosclerosis |
|
|
| Osteochondrodysplasia |
|
Skeletal Dysplasia
|
Chondrodystrophy
|
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
| Myopathy |
|
Muscular Diseases
|
Myopathies
|
|
|
| Anterior Cerebral Artery Infarction |
|
Infarction, Anterior Cerebral Artery
|
|
|
| Methylmalonic Aciduria And Homocystinuria, Cbld Type |
|
Homocystinuria, Cbld Type, Variant 1
|
Methylmalonic Aciduria And Homocystinuria Type Cbld
|
|
Vitamin B12-Responsive Methylmalonic Acidemia, Type Cbldv2
|
MAHCD
|
|
Methylmalonic Acidemia And Homocystinuria, Cbld Type
|
Methylmalonic Aciduria, Cblh Type, Formerly
|
|
Methylmalonic Acidemia, Cblh Type, Formerly
|
Methylmalonic Aciduria, Cbld Type, Variant 2
|
|
Cobalamin D Deficiency
|
Methylcobalamin Deficiency Type Cbldv1
|
|
Functional Methionine Synthase Deficiency Type Cbldv1
|
Vitamin B12-Responsive Methylmalonic Aciduria, Type Cbldv2
|
|
Methylmalonic Acidemia With Homocystinuria, Type Cbld
|
Cbld Defect
|
|
Cobalamin D Defect
|
Combined Defect In Adenosylcobalamin And Methylcobalamin Synthesis, Type Cbld
|
|
Methylmalonic Aciduria With Homocystinuria, Type Cbld
|
Homocystinuria Cbld Variant 1
|
|
Methylmalonic Acidemia And Homocystinuria Cbld Type
|
Methylmalonic Aciduria And Homocystinuria Cbld-Combined
|
|
Methylmalonic Aciduria And Homocystinuria Cbld Original
|
Methylmalonic Aciduria Cbld Variant 2
|
|
Aciduria, Methylmalonic, And Homocystinuria, Cbld Type
|
|
|
| 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
|
|
|
| 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
|
|
|
| Sensorineural Hearing Loss |
|
Sensory Hearing Loss
|
Sensorineural Deafness
|
|
Sensorineural Hearing Loss Disorder
|
Hearing Loss, Sensorineural
|
|
Central Hearing Loss
|
High Frequency Deafness
|
|
High Frequency Hearing Loss
|
High-Frequency Hearing Loss
|
|
Perceptive Deafness
|
Perceptive Hearing Loss
|
|
Perceptive Hearing Loss Or Deafness
|
Hearing Loss Sensorineural
|
|
Deafness Sensorineural
|
Hearing Loss High-Frequency
|
|
Hearing Loss, Central
|
Hearing Loss, High-Frequency
|
|
|
| Left Ventricular Noncompaction |
|
Noncompaction Cardiomyopathy
|
Left Ventricular Hypertrabeculation
|
|
Lvnc
|
Spongy Myocardium
|
|
Isolated Noncompaction Of The Ventricular Myocardium
|
Left Ventricular Myocardial Noncompaction Cardiomyopathy
|
|
Fetal Myocardium
|
Honeycomb Myocardium
|
|
Hypertrabeculation Syndrome
|
Left Ventricular Non-Compaction
|
|
Lvht
|
Non-Compaction Of The Left Ventricular Myocardium
|
|
Ventricular Noncompaction, Left
|
Non-Compaction Cardiomyopathy
|
|
|
| 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
|
|
|
