Skip to main content

Medical Subject Headings

Search from vocabulary

Content language

Concept information

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Anemia, Hemolytic, Congenital > Hemoglobin C Disease
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Anemia > Anemia, Hemolytic > Anemia, Hemolytic, Congenital > Hemoglobin C Disease
Hemic and Lymphatic Diseases > Hematologic Diseases > Hemoglobinopathies > Hemoglobin C Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Hemoglobinopathies > Hemoglobin C Disease

Preferred term

Hemoglobin C Disease  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Hemoglobin-C Disease
  • Hemoglobin-C Diseases

Note

  • a congen hemolytic anemia; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; do not confuse with HEMOGLOBIN SC DISEASE

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.

History note

  • 1972(1966)

In other languages

URI

http://www.yso.fi/onto/mesh/D006445

Download this concept:

RDF/XML TURTLE JSON-LD Created 1/1/99, last modified 2/26/23