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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
Amyotrophic Lateral Sclerosis 1
USH2A c.8559-2A>G
Cystic Fibrosis
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Common Disease
Ngly1-Congenital Disorder of Deglycosylation
Alias:
Congenital Disorder of Deglycosylation
Deficiency of N-Glycanase 1
Ngly1-Cddg
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Ngly1-Congenital Disorder of Deglycosylation, also known as congenital disorder of deglycosylation, is related to congenital disorder of deglycosylation 2 and congenital disorder of deglycosylation 1. Affiliated tissues include retina and eye.
Related ID:
MALACARDS:NGL005
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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NGL005
Medical Symptom
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HPO Source Accession
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Gene & Mutation
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Name
MGI
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