| 疾病名称 |
别名 |
|
| Hyperaldosteronism, Familial, Type Iii |
|
Familial Hyperaldosteronism Type Iii
|
Fh Iii
|
|
Fh3
|
Familial Hyperaldosteronism Type 3
|
|
HALD3
|
Fh-Iii
|
|
Hyperaldosteronism, Familial, 3
|
Familial Hyperaldosteronism 3
|
|
Fh Type Iii
|
|
|
| Long Qt Syndrome 13 |
|
LQT13
|
Qt Syndrome, Long, Type 13
|
|
|
| Andersen Cardiodysrhythmic Periodic Paralysis |
|
Andersen Syndrome
|
Andersen-Tawil Syndrome
|
|
LQT7
|
Long Qt Syndrome 7
|
|
Ats
|
Periodic Paralysis, Potassium-Sensitive Cardiodysrhythmic Type
|
|
Long Qt Syndrome Type 7
|
Andersen Tawil Syndrome
|
|
Potassium-Sensitive Cardiodysrhythmic Type
|
Lqts Type 7
|
|
Long Qt Syndrome-7
|
|
|
| Long Qt Syndrome |
|
Romano-Ward Syndrome
|
Long Q-T Syndrome
|
|
Lqt
|
Qt Syndrome, Long
|
|
Congenital Long Qt Syndrome
|
Familial Long Qt Syndrome
|
|
|
| Long Qt Syndrome 1 |
|
Romano-Ward Syndrome
|
LQT1
|
|
Ward-Romano Syndrome
|
Rws
|
|
Ventricular Fibrillation With Prolonged Qt Interval
|
Wrs
|
|
Long Qt Syndrome 1, Acquired, Susceptibility To
|
Long Qt Syndrome 1, Acquired
|
|
Romano-Ward Long Qt Syndrome
|
Long Qt Syndrome Type 1
|
|
Long Qt Syndrome-1
|
Acquired Susceptibility To Long Qt Syndrome 1
|
|
Qt Syndrome, Long, Type 1
|
|
|
| Osteoarthritis |
|
Osteoarthrosis
|
Degenerative Joint Disease
|
|
Hypertrophic Arthritis
|
Arthropathy
|
|
Degenerative Polyarthritis
|
Degenerative Arthritis
|
|
Osteoarthrosis And Allied Disorder
|
Arthritis, Degenerative
|
|
Oa
|
Osteoarthritis Deformans
|
|
Osteoarthrosis Deformans
|
Kashin-Beck Disease
|
|
|
| Neonatal Diabetes |
|
Neonatal Diabetes Mellitus
|
Diabetes Mellitus Syndrome In Newborn Infant
|
|
Ndm
|
|
|
| Hyperinsulinism |
|
|
| Adrenal Carcinoma |
|
Adrenal Cancer
|
Adrenal Gland Cancer
|
|
Malignant Neoplasm Of Adrenal Gland
|
Adrenal Gland Neoplasms
|
|
Carcinoma Of The Adrenal Gland
|
Adrenal Neoplasm
|
|
Malignant Adrenal Tumor
|
Neoplasm Of Adrenal Gland
|
|
Tumor Of The Adrenal Gland
|
Adrenal Gland Neoplasm
|
|
Adrenocortical Carcinoma
|
Adrenal Gland Malignancy
|
|
Suprarenal Cancer
|
Malignant Neoplasm Of Suprarenal Gland
|
|
Malignant Neoplasm Of Adrenal Gland, Unspecified
|
Malignant Tumour Of Adrenal Gland
|
|
Suprarenal Gland Cancer
|
Primary Malignant Neoplasm Of Adrenal Gland
|
|
|
| Hypokalemia |
|
Potassium Deficiency
|
Potassium Deficiency Disorder
|
|
Hypopotassemia
|
Potassium
|
|
Potassium [K] Deficiency
|
Hypokalaemic Syndrome
|
|
Hypopotassaemia
|
Hypopotassaemia Syndrome
|
|
Hypokalaemic
|
Potassium Depletion
|
|
|
| Hyperinsulinemic Hypoglycemia |
|
Nesidioblastosis
|
Islet Cell Hyperplasia
|
|
Persistent Hyperinsulinemia Hypoglycemia Of Infancy
|
Hyperinsulinemic Hypoglycaemia
|
|
|
| Ischemia |
|
|
| Cardiac Arrhythmia, Ankyrin-B-Related |
|
Long Qt Syndrome 4
|
Ankyrin-B Syndrome
|
|
LQT4
|
Ankyrin-B-Related Cardiac Arrhythmia
|
|
Sick Sinus Syndrome With Bradycardia
|
Arrhythmia, Cardiac, Ankyrin B-Related
|
|
|
| Adrenal Gland Disease |
|
Adrenal Gland Diseases
|
Adrenal Gland Disorders
|
|
|
| Conn'S Syndrome |
|
Cushing Syndrome
|
Hyperaldosteronism
|
|
Primary Hyperaldosteronism
|
Hypercortisolism
|
|
Primary Aldosteronism
|
Cushing'S Syndrome
|
|
Adrenal Gland Hyperfunction
|
Conn Syndrome
|
|
Hyperadrenalism
|
Ectopic Acth Syndrome
|
|
Hyperadrenocorticism
|
Cushing Disease
|
|
Cushing'S Disease
|
Adrenal Cortex Adenoma
|
|
Corticotroph Pituitary Adenoma
|
Pituitary Corticotroph Micro-Adenoma
|
|
Pituitary-Dependent Cushing Syndrome
|
Pituitary Acth Hypersecretion
|
|
Acth Syndrome, Ectopic
|
Acth-Secreting Pituitary Adenoma
|
|
Adrenal Hyperfunction Resulting From Pituitary Acth Excess
|
Ectopic Adrenocorticotropic Hormone Syndrome
|
|
Nodular Primary Adrenocortical Dysplasia
|
Pituitary Dependent Cushing Syndrome
|
|
Pituitary Cushing Syndrome
|
Pituitary-Dependant Cushing Syndrome
|
|
Pituitary-Dependant Hypercortisolism
|
Pituitary-Dependant Hypercortisolism Disorder
|
|
Aldosteronism Primary
|
Acth Syndrome Ectopic
|
|
Adrenal Cushing'S Syndrome
|
Adrenal Cortical Adenoma
|
|
Cushing Syndrome Nos
|
Cortisol Hypersecretion
|
|
Corticoadrenal Hypersecretion
|
Cushing Syndrome Secondary To Ectopic Acth-Secretion
|
|
Ectopic Cushing Syndrome
|
Hypercortisolism Due To Nonpituitary Tumour
|
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion Causing Cushing Syndrome
|
|
Idiopathic Aldosteronism
|
Aldosteronism
|
|
Primary Aldosteronism Due To Bilateral Adrenal Hyperplasia
|
Primary Aldosteronism Due To Adrenal Hyperplasia
|
|
|
| Myocardial Stunning |
|
|
| Hyperaldosteronism, Familial, Type I |
|
Glucocorticoid-Remediable Aldosteronism
|
Gra
|
|
Familial Hyperaldosteronism Type 1
|
Hyperaldosteronism, Familial Type 1
|
|
HALD1
|
Fh I
|
|
Glucocorticoid-Suppressible Hyperaldosteronism
|
Gsh
|
|
Acth-Dependent Hyperaldosteronism Syndrome
|
Aldosteronism, Glucocorticoid-Remediable
|
|
Dexamethasone Sensitive Hypertension
|
Glucocorticoid Sensitive Hypertension
|
|
Familial Hyperaldosteronism Type I
|
Fh1
|
|
Aldosteronism, Sensitive To Dexamethasone
|
Dexamethasone-Sensitive Hypertension
|
|
Fh-I
|
Glucocorticoid-Sensitive Hypertension
|
|
Hyperaldosteronism, Familial, 1
|
Aldosteronism Sensitive To Dexamethasone
|
|
Familial Hyperaldosteronism 1
|
Fh Type 1
|
|
Familial Aldosteronism Type I
|
|
|
| Hypoglycemia |
|
Hypoglycaemia
|
Low Blood Sugar
|
|
Hypoglycaemia Nos
|
Spontaneous Hypoglycaemia
|
|
Nondiabetic Hypoglycaemia
|
Hypoglycaemic Disorder Nos
|
|
Hypoglycaemic 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
|
|
|
| Long Qt Syndrome 10 |
|
LQT10
|
Atrial Fibrillation, Familial, 17
|
|
ATFB17
|
Long Qt Syndrome-10
|
|
Qt Syndrome, Long, Type 10
|
|
|
| Permanent Neonatal Diabetes Mellitus |
|
Pndm
|
Permanent Diabetes Mellitus Of Infancy
|
|
Pdmi
|
Neonatal Diabetes Mellitus, Permanent
|
|
|
| Long Qt Syndrome 11 |
|
LQT11
|
Long Qt Syndrome-11
|
|
Qt Syndrome, Long, Type 11
|
|
|
| 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
|
|
|
| Adrenal Adenoma |
|
Adenoma Of The Adrenal Gland
|
Adrenal Incidentaloma
|
|
Adrenal Cortical Adenoma
|
Adrenocortical Adenoma
|
|
|
| Vitreoretinal Degeneration, Snowflake Type |
|
Snowflake Vitreoretinal Degeneration
|
SVD
|
|
Snowflake Degeneration In Hereditary Vitreoretinal Degeneration
|
|
|
| Ventricular Fibrillation, Paroxysmal Familial, 1 |
|
Paroxysmal Familial Ventricular Fibrillation
|
Ivf
|
|
Ventricular Fibrillation, Idiopathic
|
Ventricular Fibrillation
|
|
VF1
|
Vf
|
|
Ventricular Fibrillation, Familial, 1
|
Paroxysmal Ventricular Fibrillation
|
|
Idiopathic Ventricular Fibrillation
|
Ventricular Fibrillation, Paroxysmal Familial, Type 1
|
|
Ventricular Fibrillation, Paroxysmal Familial
|
Familial Paroxysmal Ventricular Fibrillation 1
|
|
Susceptibility To Ventricular Fibrillation During Myocardial Infarction
|
Ventricular Fibrillation Adverse Event
|
|
|
| Long Qt Syndrome 9 |
|
LQT9
|
Long Qt Syndrome-9
|
|
Qt Syndrome, Long, Type 9
|
|
|
| Primary Pigmented Nodular Adrenocortical Disease |
|
Ppnad
|
Primary Pigmented Nodular Adrenal Dysplasia
|
|
Pigmented Nodular Adrenocortical Disease, Primary, 2
|
Pigmented Nodular Adrenocortical Disease, Primary, 1
|
|
|
| Long Qt Syndrome 2 |
|
LQT2
|
Long Qt Syndrome, Acquired, Reduced Susceptibility To
|
|
Long Qt Syndrome 1/2
|
Long Qt Syndrome 2/3
|
|
Long Qt Syndrome 2/5
|
Long Qt Syndrome 2, Acquired, Susceptibility To
|
|
Long Qt Syndrome, Acquired, Reduced
|
Long Qt Syndrome Type 2
|
|
Long Qt Syndrome 2/9
|
Lqt1/2
|
|
Lqt2/3
|
Lqt2/5
|
|
Lqt2/9
|
Susceptibility To Acquired Long Qt Syndrome 2
|
|
Long Qt Syndrome-2
|
Qt Syndrome, Long, Type 2
|
|
Long Qt Syndrome 1-2
|
Long Qt Syndrome 2-3
|
|
Long Qt Syndrome 2-5
|
Long Qt Syndrome 9
|
|
|
| Hyperkalemic Periodic Paralysis |
|
HYPP
|
Gamstorp Disease
|
|
Gamstorp Episodic Adynamy
|
Adynamia Episodica Hereditaria With Or Without Myotonia
|
|
Familial Hyperkalemic Periodic Paralysis
|
Hyperkpp
|
|
Hyperpp
|
Adynamia Episodica Hereditaria
|
|
Primary Hyperkalemic Periodic Paralysis
|
Hyperkalemic Periodic Paralysis, Type 2
|
|
Sodium Channel Muscle Disease
|
Familial Hyperpp
|
|
Hyperkalemic Pp
|
Primary Hyperpp
|
|
Periodic Paralysis Hyperkalemic
|
Periodic Paralysis Normokalemic
|
|
NKPP
|
Periodic Paralysis Eukalemic
|
|
Paralysis, Hyperkalemic Periodic
|
Paralysis, Periodic, Hyperkalemic
|
|
Potassium Aggravated Myotonia
|
|
|
| Short Qt Syndrome |
|
Sqts
|
Familial Short Qt Syndrome
|
|
|
| Long Qt Syndrome 3 |
|
LQT3
|
Long Qt Syndrome Type 3
|
|
Long Qt Syndrome-3
|
Qt Syndrome, Long, Type 3
|
|
|
| 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
|
|
|
| Endocrine Organ Benign Neoplasm |
|
|
| Familial Periodic Paralysis |
|
Genetic Periodic Paralysis
|
Paralyses, Familial Periodic
|
|
|
| Acth-Independent Macronodular Adrenal Hyperplasia |
|
Acth-Independent Macronodular Adrenocortical Hyperplasia
|
Adrenocorticotropic Hormone-Independent Macronodular Adrenal Hyperplasia
|
|
Corticotropin-Independent Macronodular Adrenal Hyperplasia
|
Cushing Syndrome Due To Macronodular Adrenal Hyperplasia
|
|
AIMAH1
|
Aimah
|
|
Massive Macronodular Adrenocortical Disease
|
Mmad
|
|
Primary Macronodular Adrenal Hyperplasia
|
Cushing Syndrome, Adrenal, Due To Aimah
|
|
Primary Bilateral Macronodular Adrenal Hyperplasia
|
Acth-Independent Macronodular Adrenal Hyperplasia 1
|
|
Acth-Independent Cushing Syndrome
|
Adrenal Cushing Syndrome Due To Aimah
|
|
Acth-Independent Macronodular Adrenal Hyperplasia 2
|
|
|
| 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
|
|
|
| Night Blindness, Congenital Stationary, Type 1h |
|
Congenital Stationary Night Blindness 1h
|
CSNB1H
|
|
Congenital Stationary Night Blindness Type 1h
|
Night Blindness, Congenital Stationary, 1h
|
|
|
| Hypokalemic Periodic Paralysis, Type 1 |
|
Hypokalemic Periodic Paralysis
|
Hokpp
|
|
Hypopp
|
Westphall Disease
|
|
HOKPP1
|
Familial Hypokalemic Periodic Paralysis
|
|
Familial Periodic Paralysis
|
Westphal Disease
|
|
Hypokalemic Periodic Paralysis Type 1
|
Hypokalemic Familial Periodic Paralysis
|
|
Periodic Hypokalemic Paralysis
|
Periodic Paralysis I
|
|
Hypokpp
|
Primary Hypokalemic Periodic Paralysis
|
|
Periodic Paralysis Hypokalemic 1
|
Paralysis, Hypokalemic, Periodic
|
|
Paralysis, Hypokalemic, Periodic, Type 1
|
|
|
| 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
|
|
|
| Adrenal Cortex Disease |
|
|
| Catecholaminergic Polymorphic Ventricular Tachycardia |
|
Cpvt
|
Catecholamine-Induced Polymorphic Ventricular Tachycardia
|
|
Familial Polymorphic Ventricular Tachycardia
|
Malignant Paroxysmal Ventricular Tachycardia
|
|
Multifocal Ventricular Premature Beats
|
Stress-Induced Polymorphic Ventricular Tachycardia
|
|
Bidirectional Tachycardia Induced By Catecholamine
|
Double Tachycardia Induced By Catecholamines
|
|
Polymorphic Catecholergic Ventricular Tachycardia
|
Syncopal Paroxysmal Tachycardia
|
|
Bidirectional Tachycardia Induced By Catecholamines
|
Fpvt
|
|
Bidirectional Ventricular Tachycardia Induced By Catecholamine
|
Polymorphic Ventricular Tachycardia Induced By Catecholamines
|
|
Ventricular Tachycardia, Catecholaminergic Polymorphic
|
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1
|
|
Familial Ventricular Tachycardia
|
Multifocal Pvcs
|
|
Multifocal Premature Ventricular Beats
|
|
|
| Liddle Syndrome 1 |
|
Liddle Syndrome
|
Pseudoaldosteronism
|
|
Liddle'S Syndrome
|
LIDLS1
|
|
Lidls
|
Pseudohyperaldosteronism
|
|
Pseudoprimary Hyperaldosteronism
|
Pseudohyperaldosteronism Type 1
|
|
Liddles Syndrome
|
|
|
| Familial Atrial Fibrillation |
|
Atrial Fibrillation, Familial
|
Atfb
|
|
Atrial Fibrillation Autosomal Dominant
|
Autosomal Dominant Atrial Fibrillation
|
|
Auricular Fibrillation
|
Atrial Fibrillation
|
|
Atrial Fibrillation, Familial, 1
|
|
|
| Diabetes Mellitus |
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| Adrenal Cortical Carcinoma |
|
Adrenocortical Carcinoma
|
Adrenal Cortex Carcinoma
|
|
Carcinoma Of The Adrenal Cortex
|
Acc
|
|
Adrenocortical Cancer
|
Carcinoma Adrenocortical
|
|
|
| Carney Complex Variant |
|
Carney Complex
|
Carney Syndrome
|
|
Carney Complex, Type 1
|
Lamb Syndrome
|
|
Name Syndrome
|
Myxoma-Spotty Pigmentation-Endocrine Overactivity Syndrome
|
|
Carney Complex - Trismus - Pseudocamptodactyly Syndrome
|
Carney Complex, Type 2
|
|
Car
|
Cnc1
|
|
Carney Myxoma-Endocrine Complex
|
Myxoma - Spotty Pigmentation - Endocrine Overactivity
|
|
Myxoma, Spotty Pigmentation, And Endocrine Overactivity
|
Lamb - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome
|
|
Name - Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome
|
Carney Complex-Trismus-Pseudocamptodactyly Syndrome
|
|
CACOV
|
|
|
| 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
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Sudden Unexplained Death Syndrome
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Suds
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Sunds - [Sudden Unexplained Nocturnal Death Syndrome]
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