Inborn disorder of histidine metabolism

rare

An inherited metabolic disease that is has its basis in the disruption of histidine metabolic process.

Identifiers: MONDO:0019228 Orphanet:79181
Part of: Inborn disorder of amino acid metabolism
Also known as: disorder of histidine metabolic process · disorder of histidine metabolism · disturbance of histidine metabolism · histidine metabolic process disease · histidine metabolism disease

Subtypes

Disease	ID	Subtypes	Genes
Histidinemia	MONDO:0009345	1	HAL
Urocanic aciduria	MONDO:0010167		UROC1

Rare disease

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