About: Sickle Cell Disease

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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

Attributes	Values
rdf:type	Class
rdfs:label	Sickle Cell Disease
rdfs:subClassOf	Hemoglobinopathies nodeID://b712384
Has_NICHD_Parent	Hemoglobinopathies
Concept_In_Subset	NICHD Terminology NICHD Newborn Screening Terminology NICHD Pediatric Terminology Neonatal Research Network Terminology
Semantic_Type	Disease or Syndrome
Preferred_Name	Sickle Cell Disease
UMLS_CUI	C0002895
Contributing_Source	NICHD
ALT_DEFINITION	An inherited disease in which the red blood cells have an abnormal crescent shape, block small blood vessels, and do not last as long as normal red blood cells. Sickle cell anemia is caused by a mutation (change) in one of the genes for hemoglobin (the substance inside red blood cells that binds to oxygen and carries it from the lungs to the tissues). It is most common in people of West and Central African descent.NCI-GLOSS A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S.MSH2003_2003_05_12
Legacy_Concept_Name	Sickle_Cell_Disease
FULL_SYN	Sickle Cell (SS only)PTNICHD sickle cell anemiaPTNCI-GLOSSCDR0000559458 Hemoglobin SSSYNCI sickle cell diseasePTNCI-GLOSSCDR0000546598 Hb SSSYNCI Sickle Cell AnemiaSYNCI Sickling Disorder due to Hemoglobin SSYNICHD Sickle Cell DiseasePTNCI Sickle Cell DiseasePTNICHD Hemoglobin SS DiseaseSYNCI
DEFINITION	A blood disorder characterized by the appearance of sickle-shaped red blood cells and anemia.NCI
code	C34383
http://linked.open...y/mesh/hasConcept	http://linked.opendata.cz/resource/mesh/concept/M0001140
is someValuesFrom of	nodeID://b677884 nodeID://b690408
is sameAs of	Anemia, Sickle Cell

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