Related Disorders
Synonym(s): CDG1o, CDGIo, Congenital Disorder of Glycosylation 1o, Congenital Disorder of Glycosylation Io
OMIM
* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.
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