FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

40888008: Congenital anomaly of the hematopoietic system (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
68197019 Congenital anomaly of the hematopoietic system en Synonym Active Entire term case insensitive SNOMED CT core module
492821011 Congenital anomaly of the haematopoietic system en Synonym Active Entire term case insensitive SNOMED CT core module
777613014 Congenital anomaly of the hematopoietic system (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

49 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

Back to Start