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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
Cohen Syndrome (COH1)
Alias:
Pepper Syndrome
Hypotonia, Obesity, and Prominent Incisors
Coh1
Prominent Incisors-Obesity-Hypotonia Syndrome
Hypotonia-Obesity-Prominent Incisors
Obesity-Hypotonia Syndrome
Cohen Syndrome, Type 1
Stage 4s Neuroblastoma
Chs1, Formerly
Norio Syndrome
Chs1
Coh
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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
科恩综合症,又名胡椒综合症,与粒细胞减少和中性粒细胞减少有关。与科恩综合症有关的重要基因是VPS13B(Vacuolar Protein Sorting 13 Homolog B),其相关通路/超级通路包括自噬通路。在该疾病的背景下提到了拓扑替康和粒细胞集落刺激因子。附属组织包括眼睛和骨骼,相关表型为近视和智力障碍。
Related ID:
MALACARDS:CHN016
OMIM:216550
MESH:C536438
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
胎儿期
--
22
173
134
CHN016
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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