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Arthrogryposis Multiplex Congenita-3

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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Arthrogryposis Multiplex Congenita-3 is related to arthrogryposis multiplex congenita 3, myogenic type and emery-dreifuss muscular dystrophy. An important gene associated with Arthrogryposis Multiplex Congenita-3 is SYNE1 (Spectrin Repeat Containing Nuclear Envelope Protein 1). Related phenotypes are muscle and cardiovascular system
Related ID：
MALACARDS：ART171

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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7
47
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ART171

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
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

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

References Literature

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PMID
Journal
Year
IF
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