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GTR Home > Conditions/Phenotypes > Paroxysmal nocturnal hemoglobinuria 2

Paroxysmal nocturnal hemoglobinuria 2

Summary

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

Available tests

12 tests are in the database for this condition.

Clinical tests (12 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CGI-06, MCAHS3, NDAP, PIG-T, PNH2, PIGT
    Summary: phosphatidylinositol glycan anchor biosynthesis class T

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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