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Ontology Browser

Orthostatic Hypotension 2 (DOID:9009252)
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Parent Terms Term With Siblings Child Terms
dopamine beta-hydroxylase deficiency  
Idiopathic Orthostatic Hypotension 
Orthostatic Hypotension 2  
An autosomal recessive disorder characterized by severe orthostatic hypotension, recurrent hypoglycemia, and low norepinephrine levels. The disorder has onset in infancy or early childhood. The disorder results from a defect in the biosynthesis of norepinephrine from dopamine due to a cofactor deficiency.
Orthostatic Hypotensive Disorder, Streeten Type 

Exact Synonyms: ORTHYP2
Primary IDs: OMIM:618182
Definition Sources: OMIM:618182

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