Lipodystrophy, Congenital Generalized, Type 1 (CGL1)

Alias:
Congenital Generalized Lipodystrophy Type 1
Berardinelli-Seip Congenital Lipodystrophy, Type 1
Lipodystrophy, Berardinelli-Seip Congenital, Type 1
Brunzell Syndrome, Agpat2-Related
Brunzell Syndrome Agpat2-Related
Bscl1
Cgl1
Berardinelli-Seip Congenital Lipodystrophy Type 1
Total Lipodystrophy and Acromegaloid Gigantism
Lipodystrophy, Generalized, Congenital, Type 1
Congenital Generalized Lipodystrophy 1
Familial Partial Lipodystrophy, Type 2
Familial Generalized Lipodystrophy
Lipodystrophy Berardinelli Type
Lipoatrophic Diabetes Mellitus
Berardinelli-Seip Syndrome
Lipoatrophic Diabetes
Favorite
基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
先天性全身性脂肪营养不良1型,又称先天性全身性脂肪营养不良1型,与脂肪营养不良2型和获得性全身性脂肪营养不良有关,症状包括肌肉痛。与先天性全身性脂肪营养不良1型有关的重要基因是AGPAT2(1-酰基甘油-3-磷酸O-酰转移酶2),其相关通路/超级通路包括葡萄糖/能量代谢和脂肪生成。在该疾病的背景下,已提到恩格列净和降糖药。附属组织包括骨和肝,相关表型为心肌病和肝肿大。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
8
77
38

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
微信
信息比对
科研助手
使用教程
回到顶部