/paroxysmal nocturnal hemoglobinuria 2

paroxysmal nocturnal hemoglobinuria 2

Rare Disease

MONDO:0014166

Also Known As

PIGT paroxysmal nocturnal hemoglobinuriaparoxysmal nocturnal hemoglobinuria 2paroxysmal nocturnal hemoglobinuria 2, autosomal dominant, somatic mutationparoxysmal nocturnal hemoglobinuria caused by mutation in PIGTparoxysmal nocturnal hemoglobinuria type 2PNH2

Definition

Any paroxysmal nocturnal hemoglobinuria in which the cause of the disease is a mutation in the PIGT gene.

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Associated Genes

PIGT ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:615399 ↗

GARD

GARD:15958 ↗

Related Diseases

paroxysmal nocturnal hemoglobinuria 1

MONDO:0010438

Rare

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