Phenotypes for disease #03346 (CDG2J (glycosylation, congenital disorder of, type IIj), OMIM:613489)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Diagnosis/Initial     

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Phenotype details     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Individual ID     
0000357439 neurodevelopmental disorder CDG2J severe intellectual disability, spasticity, absent speech, microcephaly, neuromotor delay Familial, autosomal recessive - - - - - Lucia Micale 00472643
0000357440 neurodevelopmental disorder CDG2J severe intellectual disability, spasticity, absent speech, microcephaly, neuromotor delay Familial, autosomal recessive - - - - - Lucia Micale 00472644
0000357475 neurodevelopmental disorder CDG2J severe intellectual disability, spasticity, absent speech, microcephaly, developmental abnormalities, neuromotor delay Familial, autosomal recessive - - - - - Lucia Micale 00472641
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