Congenital disorder of glycosylation, type IIz

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Subtype of: Congenital disorder of glycosylation
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
congenital disorder of glycosylation, type IIz
620201C5774295MONDO:0859357MONDO_0008907MONDO_0010478
CAMLG Unknown — ClinGen —
LOC100130283 Unknown
10527672 10602363 10801058 10922383 11058895 11409861 11875054 11916319 15645285 17158594 17307006 19235233 20638314 21937992 23137060 23430905 26453362 27604308 28954837 7670249 9140401 9497260 9762608 9781039 9887379
Open Targets —
SLC35A2 Unknown
23561849 24115232 25778940 27743886 29679388 30584598 30746764 30817854 33407896
Open Targets
All3 Causal0 Unknown3
Related Diseases Diseases that share the most curated genes with Congenital disorder of glycosylation, type IIz.
5 View disease cluster →
Epileptic encephalopathy, early infantile, 22 (eiee22) 1 shared geneSLC35A2 Related via 1 shared gene including SLC35A2. Congenital disorder of glycosylation type 1a 1 shared geneLOC100130283 Related via 1 shared gene including LOC100130283. Congenital disorder of glycosylation 3 shared genesSLC35A2, CAMLG, LOC100130283 Related via 3 shared genes including SLC35A2, CAMLG, LOC100130283. Hydrops fetalis 1 shared geneLOC100130283 Related via 1 shared gene including LOC100130283. X-linked complex neurodevelopmental disorder 1 shared geneSLC35A2 Related via 1 shared gene including SLC35A2.