Congenital Disorder of Glycosylation, Type I/iix (CDG-X)

Alias:
Congenital Disorder of Glycosylation, Type I-Iix
Congenital Disorder of Glycosylation Type I/iix
Cdg-X
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Disorder of Glycosylation, Type I/iix, also known as congenital disorder of glycosylation, type i-iix, is related to congenital disorder of glycosylation, type iii and cog5-congenital disorder of glycosylation. Affiliated tissues include skin and liver, and related phenotypes are seizure and abnormality of metabolism/homeostasis

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
--
--
8

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
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!
Wechat
Comparison
Al agent
Tutorials
Back to top