Glycine encephalopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
ATYPICAL GLYCINE ENCEPHALOPATHY
289863C5548198MONDO:0015010
AMT Unknown
20301531
Disgenet, GWAS catalog, Orphanet
GCSH Unknown
20301531
CTD, Disgenet, Orphanet
GLDC Unknown
20301531
Disgenet, Orphanet
GLYCINE ENCEPHALOPATHY 2
C5830559
NICN1 Unknown — Disgenet —
GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE
C4310943617301OMIM:617301
AMT Unknown
29300369 35646099 8005589 9600239
Disgenet, ClinGen
GCSH Unknown
36190515
Disgenet
GLDC Unknown
10798358 10873393 11592811 15236413 15824356 15851735 15864413 1634607 445864 8005589 9600239 9621520
Disgenet, ClinGen
SLC6A9 Unknown — CTD, Disgenet, HPO
All5 Causal4 Unknown5
Related Diseases Diseases that share the most curated genes with Glycine encephalopathy.
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multiple mitochondrial dysfunctions syndrome 7 1 shared geneGCSH Related via 1 shared gene including GCSH. Hyperglycemia 2 shared genesGLDC, AMT Related via 2 shared genes including GLDC, AMT. Osteosarcoma 1 shared geneGLDC Related via 1 shared gene including GLDC. Generalized epilepsy 1 shared geneGLDC Related via 1 shared gene including GLDC. Non-organic psychosis 1 shared geneSLC6A9 Related via 1 shared gene including SLC6A9.