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constitutional megaloblastic anemia with severe neurologic disease

Disease Summary
Associated Targets (1)
Tclin

1


GARD Rare
Uniprot Description An inborn error of metabolism, characterized by megaloblastic anemia and/or pancytopenia, severe cerebral folate deficiency, and cerebral tetrahydrobiopterin deficiency. Clinical features include variable neurologic symptoms, ranging from severe developmental delay and generalized seizures in infancy, to childhood absence epilepsy with learning difficulties, to lack of symptoms.
Mondo Term and Equivalent IDs
MONDO:0013456:  constitutional megaloblastic anemia with severe neurologic disease
GARD:0011000: 
MESH:C565095: 
Orphanet:319651: 
SCTID:124178006: