ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Hemoglobinuria, Paroxysmal

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Hemoglobinuria, Paroxysmal 8 coordinate concepts ∟ Anemia, Refractory \| ∟ Anemia, Sideroblastic \| ∟ Leukemia, Myeloid \| ∟ Anemia, Hemolytic, Autoimmune \| ∟ Anemia, Hemolytic, Congenital \| ∟ D000743Q000151* \| ∟ Favism \| ∟ Hemolytic-Uremic Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Bone Marrow Diseases ∟ Myelodysplastic Syndromes ∟ Hemoglobinuria, Paroxysmal 8 coordinate concepts ∟ Anemia, Refractory \| ∟ Anemia, Sideroblastic \| ∟ Leukemia, Myeloid \| ∟ Anemia, Hemolytic, Autoimmune \| ∟ Anemia, Hemolytic, Congenital \| ∟ D000743Q000151* \| ∟ Favism \| ∟ Hemolytic-Uremic Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Hemoglobinuria, Paroxysmal Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Bone Marrow Diseases ∟ Myelodysplastic Syndromes ∟ Hemoglobinuria, Paroxysmal Anemia, Hemolytic > Anemia > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Myelodysplastic Syndromes > Bone Marrow Diseases > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) X
historyNote*:	78; was MARCHIAFAVA-MICHELI SYNDROME 1963-77 X
onlineNote*:	use HEMOGLOBINURIA, PAROXYSMAL to search MARCHIAFAVA-MICHELI SYNDROME 1966-77 X
publicMeSHNote*:	78; was MARCHIAFAVA-MICHELI SYNDROME 1963-77 X
Scope note:	A condition characterized by the recurrence of HEMOGLOBINURIA caused by intravascular HEMOLYSIS. In cases occurring upon cold exposure (paroxysmal cold hemoglobinuria), usually after infections, there is a circulating antibody which is also a cold hemolysin. In cases occurring during or after sleep (paroxysmal nocturnal hemoglobinuria), the clonal hematopoietic stem cells exhibit a global deficiency of cell membrane proteins. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Anemia, Refractory \| Anemia, Sideroblastic \| Leukemia, Myeloid \| Anemia, Hemolytic, Autoimmune \| Anemia, Hemolytic, Congenital \| D000743Q000151* \| Favism \| Hemolytic-Uremic Syndrome X
URI:	X
Labels and equivalent concepts:	Paroksysmaalinen hemoglobinuria (fi) Marchiafavan tauti (fi, replaced) Marchiafava-Michelin tauti (fi, replaced) Paroksysmaalinen nokturnaalinen hemoglobinuria (fi, replaced) PNH (fi, replaced) Kohtauksittainen yöllinen verenpunavirtsaisuus (fi, replaced) Kohtauksittainen yöllinen hemoglobiinivirtsaisuus (fi, replaced) Hemoglobinuria, paroksysmaalinen (fi, replaced) Kohtauksittainen verenpunavirtsaisuus (fi, replaced) Kohtauksittainen hemoglobiinivirtsaisuus (fi, replaced) Hemoglobinuri, paroxysmal (sv) Paroxysmal Hemoglobinuria, Cold (en, replaced) Paroxysmal Hemoglobinuria (en, replaced) Paroxysmal Hemoglobinuria, Nocturnal (en, replaced) Marchiafava-Micheli Syndrome (en, replaced) Haemoglobinuria paroxysmalis nocturna (la-FI, replaced) Haemoglobinuria nocturna (la-FI, replaced) X
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