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

Hemoglobin C Disease

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Anemia, Hemolytic, Congenital ∟ Hemoglobin C Disease 7 coordinate concepts ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Spherocytosis, Hereditary \| ∟ Thalassemia Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Hemoglobinopathies ∟ Hemoglobin C Disease 7 coordinate concepts ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Spherocytosis, Hereditary \| ∟ Thalassemia Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Anemia, Hemolytic, Congenital ∟ Hemoglobin C Disease 7 coordinate concepts ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Spherocytosis, Hereditary \| ∟ Thalassemia Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemoglobinopathies ∟ Hemoglobin C Disease 7 coordinate concepts ∟ Anemia, Dyserythropoietic, Congenital \| ∟ Anemia, Hemolytic, Congenital Nonspherocytic \| ∟ Anemia, Sickle Cell \| ∟ Elliptocytosis, Hereditary \| ∟ Glucosephosphate Dehydrogenase Deficiency \| ∟ Spherocytosis, Hereditary \| ∟ Thalassemia X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Anemia, Hemolytic, Congenital ∟ Hemoglobin C Disease Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Hemoglobinopathies ∟ Hemoglobin C Disease Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Anemia ∟ Anemia, Hemolytic ∟ Anemia, Hemolytic, Congenital ∟ Hemoglobin C Disease Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemoglobinopathies ∟ Hemoglobin C Disease Anemia, Hemolytic, Congenital > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Hemoglobinopathies > 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) Hemoglobinopathies > 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; do not confuse with HEMOGLOBIN SC DISEASE X
historyNote*:	72(66) X
publicMeSHNote*:	72 X
Scope note:	A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1972-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Anemia, Dyserythropoietic, Congenital \| Anemia, Hemolytic, Congenital Nonspherocytic \| Anemia, Sickle Cell \| Elliptocytosis, Hereditary \| Glucosephosphate Dehydrogenase Deficiency \| Spherocytosis, Hereditary \| Thalassemia X
URI:	X
Labels and equivalent concepts:	Hemoglobiini C -sairaus (fi) Hemoglobiini C -tauti (fi, replaced) Hemoglobin C-sjukdom (sv) X
Share:	X