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

Spherocytosis, Hereditary

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Anemia, Hemolytic, Congenital ∟ Spherocytosis, Hereditary 7 coordinate concepts ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Hemoglobin C Disease \| ∟ Thalassemia Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Anemia, Hemolytic, Congenital ∟ Spherocytosis, Hereditary 7 coordinate concepts ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Hemoglobin C Disease \| ∟ Thalassemia X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Anemia, Hemolytic, Congenital ∟ Spherocytosis, Hereditary Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Anemia, Hemolytic, Congenital ∟ Spherocytosis, Hereditary Anemia, Hemolytic, Congenital > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Anemia, Hemolytic, Congenital > Anemia, Hemolytic > Anemia > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) X
Annotation:	a congen hemolytic anemia; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
Scope note:	A familial congenital hemolytic anemia characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Related term:	Anemia, Sideroblastic X
Type:	Concept X
Coordinate terms:	Anemia, Dyserythropoietic, Congenital \| Anemia, Hemolytic, Congenital Nonspherocytic \| Anemia, Sickle Cell \| Elliptocytosis, Hereditary \| Glucosephosphate Dehydrogenase Deficiency \| Hemoglobin C Disease \| Thalassemia X
URI:	X
Labels and equivalent concepts:	Perinnöllinen pallosoluisuus (fi) Synnynnäinen sferosytoosi (fi, replaced) Synnynnäinen pallosoluinen hemolyyttinen keltaisuus (fi, replaced) Synnynnäinen pallosoluanemia (fi, replaced) Periytyvä sferosytoosi (fi, replaced) Anemia, synnynnäinen pallosolu- (fi, replaced) Akoluurinen suvuittainen keltaisuus (fi, replaced) Hereditaarinen sferosytoosi (fi, replaced) Minkowski-Chauffardin oireyhtymä (fi, replaced) Perinnöllinen sferosytoosi (fi, replaced) Minkowski-Chauffardin syndrooma (fi, replaced) Akoluurinen keltaisuus (fi, replaced) Sfärocytos, ärftlig (sv) Icterus acholuricus (la-FI, replaced) Icterus familialis acholuricus (la-FI, replaced) Icterus haemolyticus sphaerocyticus congenitus (la-FI, replaced) Syndroma Minkowski-Chauffard (la-FI, replaced) Sphaerocytosis hereditaria (la-FI, replaced) X
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