363136009: Hereditary disorder of hematologic system (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary disorder of haematologic sysem	Is a	Hereditary disorder by system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary disorder of haematologic sysem	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
elliptocytose congénitale	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Selective malabsorption of cyanocobalamin	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Muscle phosphofructokinase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Uridine monophosphate hydrolase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
syndrome d'Epstein	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Pearson's syndrome	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Lecithin cholesterol acyltransferase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency (disorder)	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Chronic granulomatous disease	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary acanthocytosis (disorder)	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary methemoglobinemia, enzymatic type	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary platelet function disorder (disorder)	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudo von Willebrand disease	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary stomatocytosis	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary coagulation factor deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial erythrocytosis	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
HNSHA due to gamma glutamyl cysteine synthetase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency (disorder)	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Propionyl-CoA carboxylase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
maladie de Hand-Schüller-Christian	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassaemia	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary factor IX deficiency disease (disorder)	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
HNSHA due to hexokinase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
HNSHA due to triosephosphate isomerase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder)	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Phosphatidylcholine-sterol acyltransferase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
HNSHA due to glutathione reductase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
HNSHA due to glucose phosphate isomerase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary spherocytosis (disorder)	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
HNSHA due to phosphoglycerate kinase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to deficiency of protein 4.1	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hemolytic anemia with emphysema AND cutis laxa (disorder)	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
HNSHA due to diphosphoglycerate mutase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Glucose-6-phosphate dehydrogenase deficiency anemia	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary sideroblastic anemia	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Amino acid deficiency anemia	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial hemorrhagic diathesis	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin defect in self-association	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to abnormal protein 4.1	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
X-linked lymphoproliferative syndrome	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to alpha spectrin defect	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypoplastic anaemia	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary hypoplasminogenemia	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary dysplasminogenaemia	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Acatalasemia	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Reticular dysgenesis	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
SCID (severe combined immunodeficiency) due to absent lymphoid stem cells	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder)	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Severe combined immunodeficiency with reticular dysgenesis (disorder)	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Chronic granulomatous disease (disorder)	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial sea-blue histiocytosis	Is a	False	Hereditary disorder of haematologic sysem	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

POSSIBLY EQUIVALENT TO association reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
754926017	Hereditary disorder of hematologic system (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1772661016	Hereditary disorder of haematologic system	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1773998010	Hereditary disorder of hematologic system	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
482273018	Hereditary disorder of hematologic sysem	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
754926017	Hereditary disorder of hematologic system (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
754926017	Hereditary disorder of hematologic system (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1206547018	Hereditary disorder of haematologic sysem	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1772661016	Hereditary disorder of haematologic system	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1772661016	Hereditary disorder of haematologic system	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1773998010	Hereditary disorder of hematologic system	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1773998010	Hereditary disorder of hematologic system	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core