Congenital Myopathy 1a, Autosomal Dominant, with Malignant Hyperthermia (CMYP1A)

Alias:
Congenital Myopathy 1a, Autosomal Dominant, with Susceptibility to Malignant Hyperthermia
Central Core Disease of Muscle
Central Core Myopathy
Cmyp1a
Ccd
Moderate Multiminicore Disease with Hand Involvement
Central Core Disease
Cco
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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
先天性肌病1a,常染色体显性,伴有恶性高热,也称为先天性肌病1a,常染色体显性,伴有恶性高热易感性,与金登堡综合症和先天性肌病1b,常染色体隐性有关,症状包括全身肌肉无力。与先天性肌病1a,常染色体显性,伴有恶性高热有关的重要基因是RYR1(ryanodine receptor 1)。相关组织包括骨骼肌和皮肤,相关表型为面瘫和新生儿低张力。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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未知
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1
24
69

Medical Symptom

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

Gene & Mutation

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Gene
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Score
Mutations
No data available

Related Drugs

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Phase
No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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No Data Found!
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