Alg1-Congenital Disorder of Glycosylation (CDGIK)

Alias:
Congenital Disorder of Glycosylation Type 1k
Carbohydrate Deficient Glycoprotein Syndrome Type Ik
Mannosyltransferase 1 Deficiency
Cdg1k
Cdgik
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Alg1-Congenital Disorder of Glycosylation, also known as congenital disorder of glycosylation type 1k, is related to congenital disorder of glycosylation, type ik and congenital disorder of glycosylation, type in. An important gene associated with Alg1-Congenital Disorder of Glycosylation is ALG1 (ALG1 Chitobiosyldiphosphodolichol Beta-Mannosyltransferase). Affiliated tissues include eye and endothelial.
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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2
9
24

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
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IF
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