Agent Commons Collaborative Research

Metabolic disease involving other neurotransmitter deficiency

rare
Identifiers
MONDO:0019253 Orphanet:79219
Part of
Inborn disorder of biogenic amine metabolism and transport

Subtypes

All diseases Rare only
Disease Subtypes
Hereditary hyperekplexia 5
Butyrylcholinesterase deficiency
Folinic acid-responsive seizures

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