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congenital brain dysgenesis due to glutamine synthetase deficiency

Disease Summary
Associated Targets (1)
Tchem

1


GARD Rare
Uniprot Description Rare developmental disorder with severe brain malformation resulting in multi-organ failure and neonatal death. Glutamine is largely absent from affected patients serum, urine and cerebrospinal fluid.
Mondo Term and Equivalent IDs
MONDO:0012393:  congenital brain dysgenesis due to glutamine synthetase deficiency
GARD:0009848: 
MESH:C536832: 
Orphanet:71278: 
UMLS:C1864910: