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Arthrogryposis Multiplex Congenita 5 (AMC5)

Alias:
Arthrogryposis Multiplex Congenita-5
Amc5
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Arthrogryposis Multiplex Congenita 5, is also known as arthrogryposis multiplex congenita-5. An important gene associated with Arthrogryposis Multiplex Congenita 5 is TOR1A (Torsin Family 1 Member A). Affiliated tissues include bone marrow and skin, and related phenotypes are scoliosis and short neck
Related ID：
MALACARDS：ART167
OMIM：618947
MESH：D001176

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
1
16
3
ART167

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

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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