| 疾病名称 |
别名 |
|
| Alagille Syndrome 1 |
|
Alagille Syndrome
|
Arteriohepatic Dysplasia
|
|
Alagille-Watson Syndrome
|
Cholestasis With Peripheral Pulmonary Stenosis
|
|
Hepatic Ductular Hypoplasia
|
Alagille Syndrome Due To A Jag1 Point Mutation
|
|
ALGS1
|
Algs
|
|
Aws
|
Syndromic Bile Duct Paucity
|
|
Cardiovertebral Syndrome
|
Hepatofacioneurocardiovertebral Syndrome
|
|
Paucity Of Interlobular Bile Ducts
|
Watson-Miller Syndrome
|
|
Alagille Syndrome Due To 20p12 Microdeletion
|
Ahd
|
|
Hepatic Ductular Hypoplasia, Syndromatic
|
Watson Alagille Syndrome
|
|
Alagille'S Syndrome
|
Alagille Syndrome Due To Del(20)(P12)
|
|
Alagille Syndrome Due To Monosomy 20p12
|
Alagille-Watson Syndrome Due To Monosomy 20p12
|
|
Arteriohepatic Dysplasia Due To Monosomy 20p12
|
Syndromic Bile Duct Paucity Due To Monosomy 20p12
|
|
Alagille-Watson Syndrome Due To A Jag1 Point Mutation
|
Arteriohepatic Dysplasia Due To A Jag1 Point Mutation
|
|
Syndromic Bile Duct Paucity Due To A Jag1 Point Mutation
|
Alagille Syndrome, 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]
|
|
|
| Deafness, Congenital Heart Defects, And Posterior Embryotoxon |
|
DCHE
|
Deafness, Congenital Heart Defects, Posterior Embryotoxon
|
|
|
| Charcot-Marie-Tooth Disease, Axonal, Type 2hh |
|
CMT2HH
|
Charcot-Marie-Tooth Neuropathy, Type 2hh
|
|
Charcot-Marie-Tooth Disease 2hh
|
|
|
| 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
|
|
|
| Heart, Malformation Of |
|
|
| Atypical Coarctation Of Aorta |
|
Middle Aortic Syndrome
|
Coarctation Of The Abdominal Aorta
|
|
Mid-Aortic Dysplastic Syndrome
|
Mid-Aortic Syndrome
|
|
Midaortic Syndrome
|
Takayasu Arteritis
|
|
|
| Pulmonic Stenosis |
|
Valvular Pulmonic Stenosis
|
Congenital Pulmonary Valvar Stenosis
|
|
Congenital Stenosis Of Pulmonary Valve
|
Pulmonary Valve Stenosis
|
|
Pulmonary Stenosis
|
Congenital Pulmonary Valve Stricture
|
|
Congenital Pulmonary Valve Stenosis
|
|
|
| Cholestasis, Progressive Familial Intrahepatic, 3 |
|
PFIC3
|
Cholestasis, Progressive Familial Intrahepatic 3
|
|
Mdr3 Deficiency
|
Progressive Familial Intrahepatic Cholestasis Type 3
|
|
Progressive Familial Intrahepatic Cholestasis 3
|
Progressive Familial Intrahepatic Cholestasis With Elevated Serum Gamma-Glutamyltransferase
|
|
Cholestasis, Progressive Familial Intrahepatic, With Elevated Serum Gamma-Glutamyltransferase
|
Progressive Familial Intrahepatic Cholestasis With Elevated Serum Gama-Glutamyltransferase
|
|
Cholestasis, Intrahepatic, Familial, Progressive, Type 3
|
|
|
| Pulmonary Valve Stenosis |
|
Valvular Pulmonary Stenosis
|
Heart Valve Pulmonary Stenosis
|
|
Valvar Pulmonary Stenosis
|
Valvate Pulmonary Stenosis
|
|
Pulmonary Stenosis
|
Pulmonary Valve Stricture
|
|
Pulmonic Valve Stenosis
|
Ps - [Pulmonary Valve Stenosis]
|
|
Pvs - [Pulmonary Valve Stenosis]
|
Pulmonary Valvular Stricture
|
|
Pulmonary Valvular Stenosis
|
Pulmonary Valvular Obstruction
|
|
Pulmonary Valve Obstruction
|
Obstructed Pulmonary Valve
|
|
|
| Cholestasis |
|
Obstruction Of Bile Duct
|
Bile Duct Obstruction
|
|
Bile Occlusion
|
Extrahepatic Biliary Obstruction
|
|
Extrahepatic Bile Duct Obstruction
|
Bile Stasis
|
|
Biliary Stasis
|
Obstructive Hyperbilirubinemia
|
|
Obstructed Jaundice
|
Bile Duct Obstructed
|
|
Bile Ductal Obstruction
|
Biliary Duct Obstruction
|
|
Obstructed Bile Ductal
|
Obstructed Biliary Duct
|
|
Obstructed Biliary Ductal
|
Jaundice Regurgitation
|
|
Obstructive Jaundice
|
Cholestatic Jaundice
|
|
Cholestatic Jaundice Syndrome
|
|
|
| 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
|
|
|
| Intrahepatic Cholestasis |
|
Cholestasis, Intrahepatic
|
Neonatal Intrahepatic Cholestasis
|
|
Cholestasis Intrahepatic
|
Cholestasis Of Pregnancy
|
|
|
| Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, Type 1 |
|
Cadasil
|
Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts And Leukoencephalopathy
|
|
Casil
|
Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy
|
|
Familial Vascular Leukoencephalopathy
|
CADASIL1
|
|
Cadasil 1
|
Hereditary Multi-Infarct Dementia
|
|
Cadasil Syndrome
|
Dementia, Hereditary Multiinfarct Type
|
|
Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy 1
|
Autosomal Dominant Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy Type 1
|
|
Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts Leukoencephalopathy
|
Dementia, Hereditary Multi-Infarct Type
|
|
Hereditary Dementia, Multi-Infarct Type
|
Cerebral Autosomal Dominant Arteriopathy-Subcortical Infarcts-Leukoencephalopathy
|
|
Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, 1
|
Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy, Autosomal Dominant
|
|
Dementia Hereditary Multiinfarct Type
|
Dementia Hereditary Multi-Infarct Type
|
|
Arteriopathy, Cerebral, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy
|
|
|
| Cholestasis, Progressive Familial Intrahepatic, 1 |
|
PFIC1
|
Byler Disease
|
|
Cholestasis, Progressive Familial Intrahepatic 1
|
Progressive Familial Intrahepatic Cholestasis 1
|
|
Progressive Familial Intrahepatic Cholestasis Type 1
|
Fic1 Deficiency
|
|
Byler'S Disease
|
Cholestasis, Fatal Intrahepatic
|
|
Progressive Familial Intrahepatic Cholestasis
|
Severe Atp8b1 Deficiency
|
|
Fatal Intrahepatic Cholestasis
|
Cholestasis, Intrahepatic, Familial, Progressive, Type 1
|
|
Progressive Intrahepatic Cholestasis
|
Cholestasis, Progressive Familial Intrahepatic 3
|
|
|
| Ventricular Septal Defect |
|
Ventricular Septal Defects
|
Interventricular Septal Defect
|
|
Heart Septal Defects, Ventricular
|
Ventricular Septal Abnormality
|
|
Interventricular Septum Defect
|
Ventricular Septum Defect
|
|
Vsd - [Ventricular Septum Defect]
|
Congenital Ventricular Septal Defect
|
|
Single Ventricular Septal Defect
|
|
|
| Biliary Atresia, Extrahepatic |
|
EHBA
|
Extrahepatic Biliary Atresia
|
|
Biliary Atresia
|
|
|
| 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
|
|
|
| Hajdu-Cheney Syndrome |
|
Acroosteolysis With Osteoporosis And Changes In Skull And Mandible
|
Cheney Syndrome
|
|
Arthrodentoosteodysplasia
|
HJCYS
|
|
Serpentine Fibula-Polycystic Kidney Syndrome
|
Sfpks
|
|
Acroosteolysis Dominant Type
|
Serpentine Fibula-Polycystic Kidneys Syndrome
|
|
Arthro-Dento-Osteo Dysplasia
|
Cranioskeletal Dysplasia With Acro-Osteolysis
|
|
Familial Osteodysplasia
|
Hereditary Osteodysplasia With Acro-Osteolysis
|
|
Hcs
|
Serpentine Fibula Syndrome
|
|
Acro-Osteolysis
|
Serpentine Fibula Polycystic Kidney Syndrome
|
|
|
| Biliary Atresia |
|
Congenital Biliary Atresia
|
Isolated Biliary Atresia
|
|
Isolated Atresia Of Bile Ducts
|
Non-Syndromic Biliary Atresia
|
|
Atresia Of Bile Duct
|
Biliary Atresia, Congenital
|
|
Atresia Of Bile Ducts
|
Bile Duct Atresia
|
|
Congenital Bile Duct Atresia
|
Ba - [Biliary Atresia]
|
|
Impervious Bile Duct
|
Atresia Of Common Duct
|
|
Biliary Duct Atresia
|
Bile Ductal Atresia
|
|
Cystic Duct Atresia
|
|
|
| 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
|
|
|
| Global Developmental Delay, Absent Or Hypoplastic Corpus Callosum, And Dysmorphic Facies |
|
GDACCF
|
Developmental Disabilities
|
|
|
| Neonatal Jaundice |
|
Neonatal Hyperbilirubinemia
|
Neonatal Icterus
|
|
Jaundice Neonatal
|
Jaundice, Neonatal
|
|
Hyperbilirubinemia, Neonatal
|
|
|
| Root Resorption |
|
|
| Cone-Rod Dystrophy 19 |
|
CORD19
|
Dystrophy, Cone-Rod, Type 19
|
|
|
| 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
|
|
|
| Squamous Cell Carcinoma |
|
Epidermoid Carcinoma
|
Squamous Cell Cancer
|
|
Carcinoma, Squamous Cell
|
Squamous Cell Skin Cancer
|
|
Malignant Squamous Cell Tumor
|
Squamous Carcinoma
|
|
Squamous Cell Epithelioma
|
Carcinoma Squamous Cell
|
|
Neoplasms, Squamous Cell
|
Squamous Cell Carcinoma - Category
|
|
Malignant Squamous Cell Neoplasm
|
Squamous Cell Carcinoma Of Skin
|
|
|
| Fundus Dystrophy |
|
Retinal Dystrophy
|
Retinal Dystrophies
|
|
Dystrophy, Retinal
|
|
|
| Hemangioma |
|
|
| Adams-Oliver Syndrome |
|
Adams Oliver Syndrome
|
Aos
|
|
Congenital Scalp Defects With Distal Limb Reduction Anomalies
|
Aplasia Cutis Congenita With Terminal Transverse Limb Defects
|
|
Congenital Scalp Defects With Distal Limb Anomalies
|
Limb, Scalp And Skull Defects
|
|
Limb Scalp And Skull Defects
|
Absence Defect Of Limbs, Scalp, And Skull
|
|
|
| Spondylocostal Dysostosis |
|
Jarcho-Levin Syndrome
|
Costovertebral Dysplasia
|
|
Spondylothoracic Dysostosis
|
Spondylothoracic Dysplasia
|
|
Scdo
|
Dysostosis, Spondylocostal
|
|
|
| Cervical Squamous Cell Carcinoma |
|
Squamous Cell Carcinoma Of The Cervix Uteri
|
Squamous Cell Carcinoma Of Cervix
|
|
|
| Cholangitis, Primary Sclerosing |
|
Primary Sclerosing Cholangitis
|
PSC
|
|
Sclerosing Cholangitis
|
Cholangitis, Sclerosing
|
|
Cholangitis Primary Sclerosing
|
Psc - [Primary Sclerosing Cholangitis]
|
|
|
| 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
|
|
|
| Focal Segmental Glomerulosclerosis |
|
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome
|
Focal Glomerulosclerosis
|
|
Fsgs
|
Segmental Glomerulosclerosis
|
|
Glomerulosclerosis, Focal Segmental
|
Fgs
|
|
Focal Glomerular Sclerosis
|
Familial Idiopathic Nephrotic Syndrome
|
|
Focal Sclerosis With Hyalinosis
|
Glomerulosclerosis, Focal
|
|
Glomerulosclerosis Focal
|
Glomerulosclerosis, Segmental, Focal
|
|
Focal Segmental Glomerulosclerosis, Not Otherwise Specified
|
|
|
| Craniosynostosis |
|
Premature Closure Of Cranial Sutures
|
Craniostenosis
|
|
Craniosynostosis Syndrome
|
Cso
|
|
Craniosynostoses
|
Congenital Ossification Of Cranial Sutures
|
|
Congenital Ossification Of Sutures Of Skull
|
Craniostosis
|
|
Imperfect Fusion Of Skull
|
Congenital Imperfect Closure Skull
|
|
Imperfect Closure Skull
|
Premature Closure Cranium Sutures
|
|
Deficiency Of Craniofacial Axis
|
|
|
| Dilated Cardiomyopathy 1t |
|
Cmd1t
|
Cardiomyopathy, Dilated, 1t
|
|
|
| Heart Septal Defect |
|
Septal Defect
|
Heart Septal Defects
|
|
Cardiac Septal Defects
|
Congenital Septal Defect Of Heart
|
|
|
| Multiple Sclerosis |
|
MS
|
Multiple Sclerosis, Susceptibility To
|
|
Disseminated Sclerosis
|
Multiple Sclerosis, Disease Progression, Modifier Of
|
|
Insular Sclerosis
|
Multiple Sclerosis Modifier Of Disease Progression
|
|
Multiple Sclerosis, Susceptibility To 1
|
Multiple Sclerosis, Susceptibility To, 1
|
|
Multiple Sclerosis 1
|
Generalized Multiple Sclerosis
|
|
Multiple Sclerosis Variant
|
Multiple Sclerosis Susceptibility To
|
|
Cerebrospinal Sclerosis
|
Generalised Multiple Sclerosis
|
|
Ms - [Multiple Sclerosis]
|
Disseminated Cerebrospinal Sclerosis
|
|
Disseminated Multiple Sclerosis
|
Disseminated Nervous System Myelosclerosis
|
|
Multiple Cerebrospinal Sclerosis
|
Multiple Combined Sclerosis
|
|
Multiple Sclerosis Generalised
|
Disseminated Brain Sclerosis
|
|
Disseminated Spinal Sclerosis
|
Insular Brain Sclerosis
|
|
Miliary Brain Sclerosis
|
Multiple Combined Sclerosis Of Spinal Cord
|
|
Multiple Ascending Sclerosis
|
Multiple Brain Sclerosis
|
|
Multiple Sclerosis Of Brain Stem
|
Multiple Sclerosis Of The Brain Stem
|
|
Multiple Sclerosis Of Cord
|
Sclérose En Plaques
|
|
Plaque Sclerosis
|
Multiple Sclerosis Of The Spinal Cord
|
|
|
| Progressive Familial Intrahepatic Cholestasis |
|
Abcb4-Related Intrahepatic Cholestasis
|
Cholestasis, Progressive Familial Intrahepatic
|
|
Pfic
|
Byler Disease
|
|
Abcb11-Related Intrahepatic Cholestasis
|
Atp8b1-Related Intrahepatic Cholestasis
|
|
Bsep Deficiency
|
Byler Disease
|
|
Byler Syndrome
|
Fic1 Deficiency
|
|
Low Γ-Gt Familial Intrahepatic Cholestasis
|
Mdr3 Deficiency
|
|
Pfic
|
Cholestasis, Intrahepatic, Familial, Progressive
|
|
Pfic - [Progressive Familial Intrahepatic Cholestasis]
|
|
|
| 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
|
|
|
| Arteriovenous Malformation |
|
Arteriovenous Malformations
|
Arteriovenous Hemangioma
|
|
Cirsoid Aneurysm
|
Racemose Aneurysm
|
|
Racemose Angioma
|
Racemose Hemangioma
|
|
Congenital Arteriovenous Malformation
|
|
|
| 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
|
|
|
| Spinocerebellar Ataxia 44 |
|
|
| Dowling-Degos Disease |
|
Reticular Pigment Anomaly Of Flexures
|
Dark Dot Disease
|
|
Reticulate Acropigmentation Of Kitamura
|
Dowling-Degos Kitamura Disease
|
|
Kitamura Reticulate Acropigmentation
|
Ddd
|
|
Dowling-Degos-Kitamura Disease
|
Reticular Pigmented Anomaly Of Flexures
|
|
|
| Medulloblastoma |
|
MDB
|
Cpnet
|
|
Localized Primitive Neuroectodermal Tumor
|
Classic Medulloblastoma
|
|
Medulloblastoma Predisposition Syndrome
|
Medulloblastoma, Somatic
|
|
Brain Medulloblastoma
|
Cns Pnet
|
|
Infratentorial Primitive Neuroectodermal Tumor
|
Neuroectodermal Tumors, Primitive
|
|
Medulloblastomas
|
Desmoplastic Medulloblastoma
|
|
Medulloblastoma, With Extensive Nodularity
|
Medulloblastoma Of Unspecified Site
|
|
Medullomyoblastoma Of Unspecified Site
|
|
|
| Hypoplastic Left Heart Syndrome |
|
Hlhs
|
Heart, Hypoplastic Left, Syndrome
|
|
Hypoplasia Of The Left Heart
|
Left Heart Hypoplasia Syndrome
|
|
Hlhs - [Hypoplastic Left Heart Syndrome]
|
Hypoplasia Of Aortic Valve, In Hypoplastic Left Heart Syndrome
|
|
Atresia Of Mitral Valve, In Hypoplastic Left Heart Syndrome
|
Atresia Or Marked Hypoplasia Of Aortic Orifice Or Valve, With Hypoplasia Of Ascending Aorta And Defective Development Of Left Ventricle
|
|
Atresia Or Marked Hypoplasia, Of Aortic Orifice Or Valve, With Hypoplasia Of Ascending Aorta And Defective Development Of Left Ventricle With Mitral Valve Atresia
|
Aortic Valve Atresia, In Hypoplastic Left Heart Syndrome
|
|
Ascending Aorta Hypoplasia, In Hypoplastic Left Heart Syndrome
|
|
|
| Scoliosis |
|
|
| Spondylocostal Dysostosis 3, Autosomal Recessive |
|
SCDO3
|
Spondylocostal Dysostosis, Autosomal Recessive 3
|
|
Spondylocostal Dysostosis 3
|
Autosomal Recessive Spondylocostal Dysostosis 3
|
|
Doid:0112361
|
Dysostosis, Spondylocostal, Autosomal Recessive, Type 3
|
|
Jarcho-Levin Syndrome
|
|
|
| Double Outlet Right Ventricle |
|
Double Outlet Right Ventricle With Subpulmonary Ventricular Septal Defect
|
Taussig-Bing Syndrome
|
|
Dextrotransposition Of Aorta
|
Taussig-Bing Syndrome Or Defect
|
|
Dorv
|
Dorv With Subpulmonary Vsd
|
|
Dorv-Tga
|
Double Outlet Right Ventricle With Transposition Of The Great Arteries
|
|
Double Outlet Right Ventricle With Subpulmonary Interventricular Communication, Transposition Type
|
Taussig-Bing Heart
|
|
Taussig-Bing Malformation
|
Taussig-Bing Complex
|
|
Taussig-Bing Defect
|
Taussig-Bing
|
|
Double Outlet Right Ventricle With Remote Ventricular Septal Defect
|
Double Outlet Right Ventricle With Uncommitted Ventricular Septal Defect
|
|
Double Outlet Right Ventricle With Non-Committed Interventricular Communication
|
Double Outlet Right Ventricle With Subaortic Or Doubly Committed Interventricular Communication Without Pulmonary Stenosis
|
|
Double Outlet Right Ventricle With Subaortic Or Doubly Committed Interventricular Communication And Pulmonary Stenosis
|
|
|
| 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
|
|
|
| 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
|
|
|
| Ovarian Cancer |
|
Ovarian Carcinoma
|
Ovarian Neoplasm
|
|
Malignant Tumour Of Ovary
|
Cancer Of The Ovary
|
|
Epithelial Ovarian Cancer
|
Neoplasm Of Ovary
|
|
Ovarian Neoplasms
|
Ovarian Cancers
|
|
Malignant Neoplasm Of Ovary
|
Primary Malignant Neoplasm Of Ovary
|
|
Ovarian Cancer, Somatic
|
Malignant Ovarian Tumor
|
|
Ovary Neoplasm
|
Primary Ovarian Cancer
|
|
Tumor Of The Ovary
|
Malignant Neoplasm Of The Ovary
|
|
Malignant Tumor Of The Ovary
|
Ovarian Malignant Tumor
|
|
OC
|
Ovarian Carcinomas
|
|
Cancer, Ovarian
|
Cancer Of Ovary
|
|
Ovary Cancer
|
Ca Ovary
|
|
|
| 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
|
|
|
| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| 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
|
|
|
| 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
|
|
|
| Rasopathy |
|
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
|
| Noonan Syndrome 1 |
|
Noonan Syndrome
|
NS1
|
|
Male Turner Syndrome
|
Female Pseudo-Turner Syndrome
|
|
Turner Phenotype With Normal Karyotype
|
Noonan Syndrome With Pigmented Villonodular Synovitis
|
|
Turner'S Phenotype, Karyotype Normal
|
Familial Turner Syndrome
|
|
Noonan'S Syndrome
|
Noonan-Ehmke Syndrome
|
|
Ns
|
Pseudo-Ullrich-Turner Syndrome
|
|
Turner Syndrome In Female With X Chromosome
|
Turner-Like Syndrome
|
|
Ullrich-Noonan Syndrome
|
Noonan-Like/Multiple Giant Cell Lesion Syndrome
|
|
Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions
|
Pterygium Colli Syndrome
|
|
Noonan Syndrome, Type 1
|
Turner Syndrome, Male
|
|
|
