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encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal recessive disorder characterized by severe encephalopathy with neonatal onset, metabolic features including lactic acidosis, little or no psychomotor development, and brain abnormalities including cerebral atrophy, cysts, and white matter abnormalities.
Mondo Term and Equivalent IDs
MONDO:0060562:  encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities
UMLS:C4540052: