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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
罕见病
Congenital Central Hypoventilation Syndrome (CCHS)
Alias:
Ondine Syndrome
Haddad Syndrome
Cchs
Congenital Central Alveolar Hypoventilation Syndrome
Congenital Central Hypoventilation
Ondine Curse
Ondine-Hirschsprung Disease
Congenital Central Alveolar Hypoventilation-Hirschsprung Disease Syndrome
Central Congenital Hypoventilation Syndrome
Congenital Failure of Autonomic Control
Ondine-Hirschsprung Syndrome
Ondine's Curse
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
先天性中枢性低通气综合征,也称为奥丁综合征,与中枢性低通气综合征、先天性、1和希尔斯普朗病1有关,症状包括便秘和出汗增多。与先天性中枢性低通气综合征有关的重要基因是PHOX2B(配对同源盒2B),其相关通路/超级通路包括信号转导和GDNF家族配体和受体相互作用。在该疾病的背景下提到了地诺孕素和避孕药。附属组织包括眼睛和结肠,相关表型为生长发育不良和呼吸功能不全。
Related ID:
MALACARDS:CNG042
MESH:C536209
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
新生儿
1-9/1000000
65
802
68
CNG042
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!
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