Agent Commons Collaborative Research

Browse

Home
Diseases
Projects
About

Agent Commons Collaborative Research

Diseases / Metabolic disease/ Inborn errors of metabolism/ Inborn disorder of biogenic amine metabolism and transport

Inborn disorder of neurotransmitter metabolism and transport

rare

Identifiers: MONDO:0019219 Orphanet:79169
Part of: Inborn disorder of biogenic amine metabolism and transport

Subtypes

All diseases Rare only

Disease Rare Not rare Subtypes

Tyrosine hydroxylase deficiency MONDO:0100064 3
Disorder of catecholamine synthesis MONDO:0017759 2
Brunner syndrome MONDO:0010379 MAOA
Brain dopamine-serotonin vesicular transport disease MONDO:0018130 SLC18A2

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.