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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
Combined Oxidative Phosphorylation Deficiency 16 (COXPD16)
Alias:
Infantile Hypertrophic Cardiomyopathy Due to Mrpl44 Deficiency
Coxpd16
Combined Oxidative Phosphorylation Defect Type 16
Combined Oxidative Phosphorylation Deficiency, Type 16
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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
复合氧化磷酸化缺陷16,也称为由于mrpl44缺乏导致的婴儿肥厚型心肌病,与限制性皮肤病变有关。与复合氧化磷酸化缺陷16有关的重要基因是MRPL44(线粒体核糖体蛋白L44)。附属组织包括肝脏和骨骼肌,相关表型为肥厚型心肌病和微泡性肝脂肪变性。
Related ID:
MALACARDS:CMB042
OMIM:615395
MESH:D028361
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
5
18
6
CMB042
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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