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Arthrogryposis Multiplex Congenita-4

Alias:
Zain Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Arthrogryposis Multiplex Congenita-4, also known as zain syndrome, is related to arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum. An important gene associated with Arthrogryposis Multiplex Congenita-4 is SCYL2 (SCY1 Like Pseudokinase 2).
Related ID：
MALACARDS：ART172

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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2
10
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ART172

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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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
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IF
No Data Found!
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