900000000000526001: REPLACED BY association reference set (foundation metadata concept)

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept (foundation metadata concept)\Reference set\Association type\Historical association reference set (foundation metadata concept)\REPLACED BY association reference set (foundation metadata concept)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT model component module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

900000000001156010 REPLACED BY association reference set (foundation metadata concept) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)

900000000001157018 REPLACED BY association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
REPLACED BY association reference set (foundation metadata concept)	Is a	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
Hematology NOS	Haematology test
Hematology finding	Hematology report (record artifact)
Hematology finding	Hematology report (record artifact)
Hematology finding abnormal	Haematology test outside reference range
Hematoside	GM3-ganglioside
Hematuria NOS	Blood in urine
Hemoglobin F-Calluna	Hemoglobin F-Heather
Hemoglobin F-Iwata	Hemoglobin F-Minoo
Hemoglobin F-Kuala Lumpur	Hemoglobin F-Urumqi
Hemoglobin F-Siena	Hemoglobin F-Carlton
Hemoglobin F-Yamaguchi	Hemoglobin F-Marietta
Hemoglobin J-Kaohslung	Haemoglobin J-Kaohsiung
Hemoglobin J-Nayanza	Haemoglobin J-Nyanza
Hemoglobin S	Hemoglobin S
Hemoglobin S disease with crisis	Hemoglobin SS disease with crisis (disorder)
Hemoglobin S disease without crisis	Hemoglobin SS disease without crisis (disorder)
Hemoglobin estimation NOS	Hemoglobin level estimation
Hemoglobin variant NOS	Hemoglobin variant test
Hemoglobin very high	Hemoglobin above reference range
Hemoglobin very low	Hemoglobin below reference range (finding)
Hemolysis	Haemolysis
Hemolytic disease NOS	Hemolytic disorder
Hemolytic disease due to other isoimmunization, NEC	Hemolytic disease of fetus OR newborn due to isoimmunization (disorder)
Hemoquant feces	Evaluation of stool specimen
Hemorrhage NOS	Bleeding
Hemorrhage control by packing NOS	Packing for haemorrhage
Hemorrhage due to any device, implant AND/OR graft	Bleeding
Hemorrhagic fever with renal syndrome	A rare rodent-borne, potentially severe, hemorrhagic disease caused by Old World Hantaviruses characterized by high fever, malaise, headache, myalgia, arthralgia, backache, abdominal pain, oliguria/renal failure and systemic hemorrhagic manifestations.
Hemorrhagic nephroso-nephritis	A rare rodent-borne, potentially severe, hemorrhagic disease caused by Old World Hantaviruses characterized by high fever, malaise, headache, myalgia, arthralgia, backache, abdominal pain, oliguria/renal failure and systemic hemorrhagic manifestations.
Hemorrhoidectomy by injection	Destruction of hemorrhoids by sclerotherapy
Hemorrhoids NOS	Hemorrhoids
Hemorrhoids with other complications NOS	Hemorrhoids
Hemorrhoids without complication	Hemorrhoids
Hemostasis of unspecified organ	Control of hemorrhage
Hepadnavirus	Family Hepadnaviridae (organism)
Heparin 100unt	Product containing heparin (medicinal product)
Heparin 10unt	Product containing heparin (medicinal product)
Heparin cofactor I	Antithrombin III
Heparin sodium 100 unt/mL solution	Heparin (as porcine heparin sodium) 100 unit/mL solution for injection
Heparin sodium 1000iu/sodium chloride 0.9% infusion solution ampule	Product containing only heparin in parenteral dose form (medicinal product form)
Heparin sodium 10u/mL injection solution ampule	Heparin (as porcine heparin sodium) 10 unit/mL solution for injection
Heparin sodium 10unt/mL solution	Heparin (as porcine heparin sodium) 10 unit/mL solution for injection
Heparin sodium in 0.9% sodium chloride 1000iu/500mL infusion	Product containing only heparin in parenteral dose form (medicinal product form)
Hepatectomy	Excision of liver (procedure)
Hepatic colic	Biliary colic
Hepatic failure as a complication of care	Hepatic failure
Hepatitis B group virus	Genus Orthohepadnavirus (organism)
Hepatitis B immunoglobulin 1000iu powder for injection solution vial	Hepatitis B surface antigen immunoglobulin-containing product in parenteral dose form
Hepatitis B immunoglobulin 200iu powder for injection solution vial	Hepatitis B surface antigen immunoglobulin-containing product in parenteral dose form
Hepatitis B immunoglobulin 500iu powder for injection solution vial	Hepatitis B surface antigen immunoglobulin-containing product in parenteral dose form
Hepatitis B screening test	Hepatitis B screening
Hepatitis B screening test	Hepatitis B screening
Hepatitis B screening test	Hepatitis B screening
Hepatitis b immune globulin 217u injection solution vial	Hepatitis B surface antigen immunoglobulin-containing product in parenteral dose form
Hepatitis b immune globulin 312units/mL injection solution 1mL vial	Hepatitis B surface antigen immunoglobulin 312 unit/mL solution for injection
Hepatitis b immune globulin 312units/mL injection solution 5mL vial	Hepatitis B surface antigen immunoglobulin 312 unit/mL solution for injection
Hepatitis caused by Toxoplasma	Hepatitis caused by Toxoplasma gondii
Hepatitis non-A non-B	Viral hepatitis
Hepatitis panel	Hepatitis panel measurement
Hepatorenal syndrome as a complication of care	Hepatorenal syndrome due to a procedure
Herbaspirillum rubrisualbicans	Herbaspirillum rubrisubalbicans (organism)
Hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome	A rare genetic cerebral small vessel disease characterized by progressive loss of visual acuity due to retinal vasculopathy, in combination with more variable neurological signs and symptoms including stroke, cognitive decline, migraine-like headaches, and seizures, among others, typically beginning in middle age. Psychiatric features such as depression and anxiety may also occur. Systemic vascular involvement with Raynaud phenomenon, micronodular liver cirrhosis, and glomerular kidney dysfunction is present in a subset of patients.
Hereditary malignant neuroendocrine neoplasm of small intestine	Hereditary well-differentiated neuroendocrine tumor of small intestine (disorder)
Hereditary methemoglobinemia, enzymatic type	A rare red cell disorder classified principally into two clinical phenotypes: autosomal recessive congenital (or hereditary) types I and II (RCM/RHM type 1; RCM/RHM type 2). In RCM type 1, cyanosis from birth is the only symptom. RCM type 2 is much more severe; the cyanosis is accompanied by neurological dysfunction (with intellectual deficit, microcephaly, growth retardation, opisthotonus, strabismus and hypertonia), which usually becomes evident during the first four months of life. RCM type 1 is caused by mutations of the CYB5R3 gene (22q13.31-qter) encoding the NADH-cytochrome b5 reductase (Cb5R) and Cb5R deficiency is limited to the erythrocytes. RCM type 2 is caused by global loss of Cb5R function. RCM type 1 is generally associated with missense mutations, whereas RCM type 2 is more commonly associated with truncating mutations, splicing errors or mutations that lead to disruption of the active site.
Hereditary nephrogenic diabetes insipidus	Hereditary vasopressin resistance
Hereditary neuraxial edema	Cerebral oedema
Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency	Glycogen storage disease due to aldolase A deficiency is an extremely rare glycogen storage disease characterized by hemolytic anemia with or without myopathy or intellectual deficit. Myopathy can be severe enough to result in fatal rhabdomyolysis in some patients. A family with episodic rhabdomyolysis (triggered by fever) without hemolytic anemia has recently been reported.
Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide-methemoglobin reductase deficiency	A rare red cell disorder classified principally into two clinical phenotypes: autosomal recessive congenital (or hereditary) types I and II (RCM/RHM type 1; RCM/RHM type 2). In RCM type 1, cyanosis from birth is the only symptom. RCM type 2 is much more severe; the cyanosis is accompanied by neurological dysfunction (with intellectual deficit, microcephaly, growth retardation, opisthotonus, strabismus and hypertonia), which usually becomes evident during the first four months of life. RCM type 1 is caused by mutations of the CYB5R3 gene (22q13.31-qter) encoding the NADH-cytochrome b5 reductase (Cb5R) and Cb5R deficiency is limited to the erythrocytes. RCM type 2 is caused by global loss of Cb5R function. RCM type 1 is generally associated with missense mutations, whereas RCM type 2 is more commonly associated with truncating mutations, splicing errors or mutations that lead to disruption of the active site.
Hereditary sensory-motor neuropathy, type V	Hereditary motor and sensory neuropathy type 5 is a rare axonal hereditary motor and sensory neuropathy characterized by slowly progressive distal muscle weakness and atrophy with or without sensory loss resulting in difficulty in walking, foot drop and pes cavus, that may be associated with pyramidal signs (extensor plantar responses, mild increase in tone, brisk tendon reflexes), muscle cramps, pain and spasticity.
Hereditary site-specific ovarian cancer syndrome	A genetic condition characterized by hereditary susceptibility to breast and/or ovarian cancer. It can be defined using family history criteria, or through identification of germline pathogenic variants (GPVs) in clinically validated HBOC genes. However, the genetic basis of about half of clinical HBOC is currently unknown or unexplained by single-gene variants, and approximately half of individuals who harbor PVs in HBOC genes do not have a suggestive family history.
Hereditary thrombocytopenia NEC	Hereditary thrombocytopenic disorder (disorder)
Hereditary vascular retinopathy	A rare genetic cerebral small vessel disease characterized by progressive loss of visual acuity due to retinal vasculopathy, in combination with more variable neurological signs and symptoms including stroke, cognitive decline, migraine-like headaches, and seizures, among others, typically beginning in middle age. Psychiatric features such as depression and anxiety may also occur. Systemic vascular involvement with Raynaud phenomenon, micronodular liver cirrhosis, and glomerular kidney dysfunction is present in a subset of patients.
Hermaphroditism	Ovotesticular disorder of sex development
Hermaphroditism	Ovotesticular disorder of sex development
Heroin - non-pharmaceutical	Diamorphine (substance)
Herpailurus yaguarondi	Puma yagouaroundi (organism)
Herpes simplex - other	Herpes simplex
Herpes simplex - other	Herpes simplex
Herpes simplex with complication	Herpes simplex
Herpes simplex with other specified complications	Herpes simplex
Herpes simplex with unspecified complications	Herpes simplex
Herpes simplex without complication	Herpes simplex
Herpes zoster with complication	Herpes zoster
Herpes zoster with nervous system complication	Herpes zoster
Herpes zoster with ophthalmic complication	Herpes zoster ophthalmicus
Herpes zoster with other central nervous system complication	Herpes zoster
Herpes zoster with other central nervous system complication	Herpes zoster
Herpes zoster with other central nervous system complication NOS	Herpes zoster
Herpes zoster with other complications	Herpes zoster
Herpes zoster with other nervous system complications	Herpes zoster
Herpes zoster with other ophthalmic complication	Herpes zoster ophthalmicus
Herpes zoster with other specified complication	Herpes zoster
Herpes zoster with other specified complication NOS	Herpes zoster
Herpes zoster with unspecified complication	Herpes zoster
Herpes zoster without complication	Herpes zoster
Herring - dietary	Herring (substance)
Hetastarch 6%	Hetastarch 60 mg/mL solution for injection
Hetastarch 6% infusion solution bottle	Hetastarch 60 mg/mL solution for injection
Hetastarch 6g liquid	Hetastarch 60 mg/mL solution for injection
Hetastarch allergy	Non-allergic hypersensitivity to hetastarch (finding)
Hexahydrophtalic anhydrid specific extract	Hexahydrophthalic anhydride (substance)

Start Previous Page 83 of 235 Next End

Reference Sets

Reference set descriptor

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
900000000001156010	REPLACED BY association reference set (foundation metadata concept)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001157018	REPLACED BY association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)