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40888008: Congenital anomaly of the hematopoietic system (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
68197019 Congenital anomaly of the hematopoietic system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
492821011 Congenital anomaly of the haematopoietic system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
777613014 Congenital anomaly of the hematopoietic system (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
68197019 Congenital anomaly of the hematopoietic system en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
68197019 Congenital anomaly of the hematopoietic system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
492821011 Congenital anomaly of the haematopoietic system en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
492821011 Congenital anomaly of the haematopoietic system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
777613014 Congenital anomaly of the hematopoietic system (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
777613014 Congenital anomaly of the hematopoietic system (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
921051000195110 anomalia congenita del sistema ematopoietico it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
499271000274117 Angeborene Fehlbildung des hämatopoetischen Systems de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
123231000077110 anomalie congénitale du système hématopoïétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
123231000077110 anomalie congénitale du système hématopoïétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
921051000195110 anomalia congenita del sistema ematopoietico it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
499271000274117 Angeborene Fehlbildung des hämatopoetischen Systems de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

51 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital anomaly of the haematopoietic system Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of the haematopoietic system Is a Disorder of hematopoietic system (navigational concept) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of the haematopoietic system Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of the haematopoietic system Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of the haematopoietic system Is a Disorder of hematopoietic structure (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of the haematopoietic system Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of the haematopoietic system Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of the haematopoietic system Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of the haematopoietic system Is a Congenital anomaly false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of the haematopoietic system Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of the haematopoietic system Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of the haematopoietic system Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of the haematopoietic system Is a Congenital malformation true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of the haematopoietic system Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of the haematopoietic system Finding site Hematopoietic system structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of the haematopoietic system Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of the haematopoietic system Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
thrombocytopénie congénitale Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Selective malabsorption of cyanocobalamin Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Muscle phosphofructokinase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Uridine monophosphate hydrolase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Pearson's syndrome Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Lecithin cholesterol acyltransferase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Chédiak-Higashi syndrome Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital atransferrinemia (disorder) Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency (disorder) Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Reticular dysgenesis Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Chronic granulomatous disease Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Erythrocytosis due to cyanotic congenital heart disease Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Familial erythrocytosis due to diphosphoglycerate mutase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Bilateral right-sidedness sequence Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
SCID (severe combined immunodeficiency) due to absent lymphoid stem cells Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to gamma glutamyl cysteine synthetase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Wiskott-Aldrich syndrome Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Propionyl-CoA carboxylase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
maladie de Hand-Schüller-Christian Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to triosephosphate isomerase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Phosphatidylcholine-sterol acyltransferase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to glutathione reductase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to glucose phosphate isomerase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of spleen Is a True Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to phosphoglycerate kinase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Hemolytic anemia with emphysema AND cutis laxa (disorder) Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to diphosphoglycerate mutase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Glucose-6-phosphate dehydrogenase deficiency anemia Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary sideroblastic anemia Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anemia Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Amino acid deficiency anemia Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
X-linked lymphoproliferative syndrome Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Radial aplasia-thrombocytopenia syndrome Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Kasabach-Merritt syndrome Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Shwachman syndrome Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital neutropenia Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Hermansky-Pudlak syndrome Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital immunodeficiency involving the hematopoietic system (disorder) Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Kernicterus due to isoimmunization Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Acatalasemia Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Severe combined immunodeficiency with reticular dysgenesis (disorder) Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Chronic granulomatous disease (disorder) Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Diaphyseal dysplasia with anaemia Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Familial sea-blue histiocytosis Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
elliptocytose congénitale Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital transferrin deficiency (disorder) Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
purpura thrombopénique congénital Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Amegakaryocytic thrombocytopenia with congenital malformation Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Leukozytenadhäsionsdefekt Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Plummer-Vinson syndrome Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Kasabach-Merritt syndrome Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital folate malabsorption anaemia Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital deficiency of intrinsic factor Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Biermer's congenital pernicious anemia Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pure red cell aplasia Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital red cell hypoplasia Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital methemoglobinemia Is a False Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of the thymus (disorder) Is a True Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital asymmetry of tonsils Is a True Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplastic anaemia Is a True Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Constitutional aplastic anaemia Is a True Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pulmonary lymphatic dysplasia syndrome (disorder) Is a True Congenital anomaly of the haematopoietic system Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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