Disease #01061

Official abbreviation PNH-1
Name hemoglobinuria, nocturnal, paroxysmal, somatic, type 1 (PNH-1)
OMIM ID 300818
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 0
Associated with 1 gene PIGA
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Disease features -
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Individuals

1 entry on 1 page. Showing entry 1.
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00028953 - PubMed: Nafa et al 1998 Patient with paroxysmal nocturnal hemoglobinuria (OMIM: 300818).Three somatic mutations were found in this patient before bone marrow transplantation, and one novel somatic mutation was found after treatment. M - - - - 0 - - PNH-1 - PIGA PIGA 5 1 Philippe Campeau
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