Congenital Disorder of Glycosylation, Type Iw, Autosomal Recessive (CDG1WAR)

Alias:
Cdg1war
Congenital Disorder of Glycosylation 1w, Autosomal Recessive
Glycosylation, Congenital Disorder of, Type Iw
Congenital Disorder of Glycosylation Type 1w
Congenital Disorder of Glycosylation Type Iw
Stt3a-Congenital Disorder of Glycosylation
Cdg Syndrome Type Iw
Stt3a-Cdg
Cdg-Iw
Cdg1w
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Disorder of Glycosylation, Type Iw, Autosomal Recessive, also known as cdg1war, is related to congenital disorder of glycosylation, type iw, autosomal dominant and stt3a-cdg and stt3b-cdg. An important gene associated with Congenital Disorder of Glycosylation, Type Iw, Autosomal Recessive is STT3A (STT3 Oligosaccharyltransferase Complex Catalytic Subunit A). Related phenotypes are intellectual disability and seizure
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
<1/1000000
1
2
2

Medical Symptom

#
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
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