| 疾病名称 |
别名 |
|
| Lipodystrophy, Familial Partial, Type 6 |
|
FPLD6
|
Lipe-Related Familial Partial Lipodystrophy
|
|
Familial Partial Lipodystrophy Type 6
|
Lipe-Related Fpld
|
|
Lipodystrophy, Familial Partial, Associated With Lipe Mutations
|
Familial Partial Lipodystrophy Associated With Lipe Mutations
|
|
Lipodystrophy, Familial Partial, 6
|
|
|
| Familial Partial Lipodystrophy |
|
Lipodystrophy, Familial Partial
|
Fpld
|
|
Kobberling-Dunnigan Syndrome
|
Dunnigan Syndrome
|
|
Koberling-Dunnigan Syndrome
|
Dunnigan-Kobberling Syndrome
|
|
Fpl
|
Familial Partial Lipodystrophy, Type 2
|
|
|
| Hyperlipidemia, Familial Combined, 3 |
|
Familial Combined Hyperlipidemia
|
Combined Hyperlipidemia, Familial
|
|
Mixed Hyperlipidaemia
|
FCHL3
|
|
Hyperlipidemia, Familial Combined
|
Familial Multiple Lipoprotein-Type Hyperlipidemia
|
|
Hyperbetalipoproteinemia With Prebetalipoproteinemia
|
Type Iib Hyperlipoproteinemia
|
|
Hyperlipidemia Familial Combined
|
Hyperlipoproteinemia Type Iib
|
|
Mixed Hyperlipemia
|
Hyperlipidaemia, Group C
|
|
Familial Hypercholesterolaemia With Hyperlipaemia
|
Familial Hyperbetalipoproteinaemia And Hyperprebetalipoproteinaemia
|
|
Hyperbetalipoproteinaemia With Prebetalipoproteinaemia
|
Hypercholesterolaemia With Endogenous Hyperglyceridaemia
|
|
Prebetalipoproteinemia Hyperbetalipoproteinaemia
|
Remnant Hyperlipoproteinemia
|
|
|
| Lipomatosis |
|
Benign Symmetrical Lipomatosis
|
|
|
| Lipodystrophy, Familial Partial, Type 5 |
|
FPLD5
|
Cidec-Related Familial Partial Lipodystrophy
|
|
Familial Partial Lipodystrophy Type 5
|
Cidec-Related Fpld
|
|
Familial Partial Lipodystrophy Associated With Cidec Mutations
|
Lipodystrophy, Familial Partial, Associated With Cidec Mutations
|
|
Lipodystrophy, Familial Partial, 5
|
|
|
| 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
|
|
|
| Chanarin-Dorfman Syndrome |
|
Neutral Lipid Storage Disease
|
CDS
|
|
Neutral Lipid Storage Disease With Ichthyosis
|
Triglyceride Storage Disease With Impaired Long-Chain Fatty Acid Oxidation
|
|
Triglyceride Storage Disease With Ichthyosis
|
Nlsdi
|
|
Ichthyotic Neutral Lipid Storage Disease
|
Dorfman-Chanarin Syndrome
|
|
Dcs
|
Chanarin-Dorfman Disease
|
|
Ichthyosiform Erythroderma With Leukocyte Vacuolation
|
Lipidosis With Triglyceride Storage Disease
|
|
Disorder Of Cornification 12
|
Dorfman Chanarin Syndrome
|
|
Neutral Lipid Storage Disease With Ichthyotic
|
Dorfman-Chanarin Disease
|
|
|
| Lipodystrophy, Familial Partial, Type 4 |
|
FPLD4
|
Plin1-Related Familial Partial Lipodystrophy
|
|
Familial Partial Lipodystrophy Type 4
|
Familial Partial Lipodystrophy Associated With Plin1 Mutations
|
|
Plin1-Related Fpld
|
Lipodystrophy, Familial Partial, Associated With Plin1 Mutations
|
|
Lipodystrophy, Familial Partial, 4
|
|
|
| Body Mass Index Quantitative Trait Locus 11 |
|
OBESITY
|
Obesity, Susceptibility To
|
|
Leanness, Inherited
|
Obesity, Susceptibility To, Bmiq11
|
|
Obesity, Mild, Early-Onset
|
Obesity, Association With
|
|
Obesity, Early-Onset, Susceptibility To
|
Obesity, Severe
|
|
Obesity, Severe, And Type Ii Diabetes
|
Obesity, Late-Onset
|
|
Obesity , Susceptibility To
|
BMIQ11
|
|
Obesity Bmiq11
|
Obesity, Early-Onset
|
|
Simple Obesity Nos
|
Excess Fat
|
|
Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified
|
Adiposis
|
|
|
| Lipodystrophy, Familial Partial, Type 2 |
|
FPLD2
|
Lipoatrophic Diabetes
|
|
Familial Partial Lipodystrophy Type 2
|
Familial Partial Lipodystrophy, Dunnigan Type
|
|
Fpl2
|
Lipoatrophic Diabetes Mellitus
|
|
Lipodystrophy, Familial Partial, Dunnigan Type
|
Lipodystrophy, Familial, Of Limbs And Lower Trunk
|
|
Lipodystrophy, Reverse Partial
|
Familial Partial Lipodystrophy Dunnigan Type
|
|
Dunnigan Syndrome
|
Familial Lipodystrophy Of Limbs And Lower Trunk
|
|
Reverse Partial Lipodystrophy
|
Lipodystrophy, Familial Partial, 2
|
|
Generalized Lipoatrophy Associated With Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy And Leukomelanodermic Papules
|
Lipodystrophy Familial Of Limbs And Lower Trunk
|
|
Lipodystrophy Reverse Partial
|
Diabetes Mellitus, Lipoatrophic
|
|
Familial Partial Lipodystrophy, Type 2
|
Familial Generalized Lipodystrophy
|
|
|
| Hyperinsulinism |
|
|
| Lipomatosis, Multiple Symmetric |
|
Multiple Symmetric Lipomatosis
|
Lipomatosis, Familial Benign Cervical
|
|
Lipomatosis, Multiple Symmetrical
|
Lipodystrophy, Cephalothoracic
|
|
Benign Symmetrical Lipomatosis
|
Madelung Disease
|
|
Madelung'S Disease
|
MSL
|
|
Cervical Symmetrical Lipomatosis
|
Launois-Bensaude'S Lipomatosis
|
|
Madelung'S Neck
|
Multiple Symmetrical Lipomatosis
|
|
Familial Symmetric Lipomatosis
|
Launois-Bensaude Syndrome
|
|
Cephalothoracic Lipodystrophy
|
Familial Benign Cervical Lipomatosis
|
|
Launois-Bensaude Lipomatosis
|
|
|
| Lipid Metabolism Disorder |
|
Dyslipidemia
|
Disorder Of Fatty Acid Metabolism
|
|
Lipid Metabolism Disorders
|
Fatty Acid Metabolism Disorder
|
|
Disorder Of Lipid Metabolism
|
Abnormality Of Lipid Metabolism
|
|
Lipid Metabolism, Inborn Errors
|
Dyslipidemias
|
|
Disorders Of Lipid Metabolism
|
Congenital Disorders Of Lipid Metabolism
|
|
Inherited Disorders Of Lipid Metabolism
|
|
|
| Lipodystrophy, Familial Partial, Type 3 |
|
FPLD3
|
Pparg-Related Familial Partial Lipodystrophy
|
|
Familial Partial Lipodystrophy Type 3
|
Familial Partial Lipodystrophy Associated With Pparg Mutations
|
|
Pparg-Related Fpld
|
Lipodystrophy, Familial Partial, Associated With Pparg Mutations
|
|
Insulin Resistance, Severe, Digenic
|
Lipodystrophy, Familial Partial, 3
|
|
Familial Partial Lipodystrophy, Type 3
|
|
|
| Leptin Deficiency Or Dysfunction |
|
Morbid Obesity
|
Obesity Due To Congenital Leptin Deficiency
|
|
LEPD
|
Congenital Leptin Deficiency
|
|
Obesity, Morbid
|
Obesity, Morbid, Due To Leptin Deficiency
|
|
Severe Obesity
|
Obesity, Morbid, Nonsyndromic 1
|
|
Leptin Deficiency
|
Obesity, Severe, Due To Leptin Deficiency
|
|
Leptin
|
Morbid Obesity Due To Leptin Deficiency
|
|
Obesity Morbid
|
Leptin Dysfunction
|
|
|
| Lysosomal Acid Lipase Deficiency |
|
Wolman Disease
|
Cholesteryl Ester Storage Disease
|
|
Lal Deficiency
|
Lipa Deficiency
|
|
Cholesterol Ester Storage Disease
|
CESD
|
|
Cholesterol Ester Hydrolase Deficiency
|
Acid Lipase Deficiency
|
|
Acid Esterase Deficiency
|
Familial Xanthomatosis
|
|
Wolman Xanthomatosis
|
Wolman'S Disease
|
|
Wolman'S Or Triglyceride Storage Type Iii Disease
|
Xanthomatosis, Familial
|
|
Liposomal Acid Lipase Deficiency, Wolman Type
|
Familial Visceral Xanthomatosis
|
|
Primary Familial Xanthomatosis
|
Primary Familial Xanthomatosis With Adrenal Calcification
|
|
Acid Lipase Disease
|
WOD
|
|
Acid Cholesteryl Ester Hydrolase Deficiency, Type 2
|
|
|
| Lysosomal And Lipase Deficiency |
|
|
| Diabetes Mellitus |
|
|
| Overnutrition |
|
|
| Acquired Metabolic Disease |
|
|
| Congenital Generalized Lipodystrophy |
|
Berardinelli-Seip Congenital Lipodystrophy
|
Berardinelli-Seip Syndrome
|
|
Brunzell Syndrome
|
Bscl
|
|
Generalized Lipodystrophy
|
Lipodystrophy, Congenital Generalized
|
|
Seip Syndrome
|
Total Lipodystrophy
|
|
Cgl
|
Lipoatrophic Diabetes
|
|
Lipodystrophy, Generalized, Congenital
|
Familial Generalized Lipodystrophy
|
|
Congenital Generalized Lipodystrophy Type 2
|
Lipoatrophic Diabetes Mellitus
|
|
Familial Partial Lipodystrophy, Type 2
|
|
|
