900000000000523009: POSSIBLY EQUIVALENT TO 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)\POSSIBLY EQUIVALENT TO 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

900000000001150016 POSSIBLY EQUIVALENT TO 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)
900000000001151017 POSSIBLY EQUIVALENT TO 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
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)	Is a	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
Hereditary disease in family possibly affecting fetus	Family history of hereditary disease (situation)
Hereditary disease in family possibly affecting fetus	Fetal hereditary disease suspected
Hereditary disorder of hematologic system	Hereditary disorder of cellular element of blood (disorder)
Hereditary disturbances in tooth structure	Hereditary disorder of tooth
Hereditary edema of legs	Hereditary lymphedema type I (disorder)
Hereditary edema of legs	Hereditary lymphedema type I (disorder)
Hereditary edema of legs	Hereditary lymphedema
Hereditary edema of legs	Hereditary lymphedema
Hereditary epistaxis	Bleeding from nose
Hereditary epistaxis	Hereditary disease
Hereditary hypertyrosinemia	Adverse reaction to ganglion blocking drug
Hereditary hypertyrosinemia	Hereditary hypertyrosinemia
Hereditary hypertyrosinemia	Deficiency of fumarylacetoacetase
Hereditary inflammatory disorder involving skin	Hereditary periodic fever (disorder)
Hereditary lentiginosis	Familial generalized lentiginosis is a rare, inherited, skin hyperpigmentation disorder characterized by widespread lentigines without associated noncutaneous abnormalities. Patients present multiple brown to dark brown, non-elevated macula of 0.2 to 1 cm in diameter, spread over the entire body, sometimes including palms or soles, but never oral mucosa.
Hereditary lentiginosis	Noonan's syndrome
Hereditary motor and sensory neuropathy	Hereditary motor and sensory neuropathy (disorder)
Hereditary motor and sensory neuropathy	Hereditary peripheral neuropathy
Hereditary motor and sensory neuropathy	Hereditary motor and sensory neuropathy (disorder)
Hereditary motor and sensory neuropathy	Hereditary motor and sensory neuropathy (disorder)
Hereditary motor and sensory neuropathy	Hereditary peripheral neuropathy
Hereditary motor and sensory neuropathy	Hereditary peripheral neuropathy
Hereditary motor and sensory neuropathy	Hereditary peripheral neuropathy
Hereditary motor and sensory neuropathy	Hereditary motor and sensory neuropathy (disorder)
Hereditary motor and sensory neuropathy	Hereditary peripheral neuropathy
Hereditary motor and sensory neuropathy	Hereditary motor and sensory neuropathy (disorder)
Hereditary myositis ossificans	Progressive myositis ossificans
Hereditary nephritis	Thin basement membrane disease
Hereditary nephropathy not elsewhere classified	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, dense deposit disease	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, diffuse crescentic glomerulonephritis	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, diffuse endocapillary proliferative glomerulonephritis	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, diffuse membranous glomerulonephritis	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, diffuse mesangial proliferative glomerulonephritis	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, diffuse mesangiocapillary glomerulonephritis	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, focal and segmental glomerular lesions	Hereditary nephropathy (disorder)
Hereditary nephropathy, not elsewhere classified, minor glomerular abnormality	Hereditary nephropathy (disorder)
Hereditary optic atrophy: [NOS] or [Leber's]	Leber's optic atrophy
Hereditary or idiopathic disturbance of tooth structure	Hereditary disorder of tooth
Hereditary or idiopathic disturbance of tooth structure	Idiopathic resorption of root of tooth (disorder)
Hereditary or idiopathic disturbance of tooth structure	Idiopathic erosion of teeth
Hereditary or idiopathic peripheral neuropathy NOS	Hereditary peripheral neuropathy
Hereditary or idiopathic peripheral neuropathy NOS	Idiopathic peripheral neuropathy
Hereditary sensory and autonomic neuropathy, type I	Charcot-Marie-Tooth disease, type I (disorder)
Hereditary sensory and autonomic neuropathy, type I	Hereditary sensory and autonomic neuropathy type I (disorder)
Hereditary sensory and autonomic neuropathy, type II	Hereditary sensory and autonomic neuropathy type II (disorder)
Hereditary sensory and autonomic neuropathy, type II	Hereditary insensitivity to pain with anhidrosis (disorder)
Hereditary sensory and autonomic neuropathy, type II	Charcot-Marie-Tooth disease, type II (disorder)
Hereditary sideroblastic anemia	A constitutional microcytic, hypochromic anemia of varying severity that is clinically characterized by manifestations of anemia and iron overload and that may respond to treatment with pyridoxine and folic acid.
Hereditary tooth structure disturbances NEC	Hereditary disorder of tooth
Hereditary tooth structure disturbances NEC	Tooth disorder
Hereditary tooth structure disturbances NEC NOS	Tooth disorder
Hereditary tooth structure disturbances NEC NOS	Hereditary disorder of tooth
Hereditary trophedema	Hereditary lymphedema
Hereditary trophedema	Hereditary lymphedema type I (disorder)
Hereditary vitamin D dependency syndrome	Vitamin D-dependent rickets
Hereditary vitamin D dependency syndrome type, II	Vitamin D-dependent rickets, type 2
Hereditary vitamin D dependency syndrome, type I	Vitamin D-dependent rickets, type 1
Hermaphroditic fluke infection	Trematode infection
Hernia	Hernial opening (morphologic abnormality)
Hernia	Herniated structure (morphologic abnormality)
Hernia - lesion	Hernial opening (morphologic abnormality)
Hernia - lesion	Herniated structure (morphologic abnormality)
Hernia of abdominal cavity	Hernia of abdominal cavity
Hernia of anterior abdominal wall without obstruction AND without gangrene	Hernia of anterior abdominal wall (disorder)
Hernia repair: [other ventral] or [epigastric] or [ventral NOS]	Repair of ventral hernia (procedure)
Hernia repair: [other ventral] or [epigastric] or [ventral NOS]	Repair of epigastric hernia
Hernia repair: [other ventral] or [epigastric] or [ventral NOS]	Repair of epigastric hernia
Hernia repair: [other] or [diaphragmatic]	Repair of diaphragmatic hernia
Hernia repair: [other] or [diaphragmatic]	Body wall and cavity procedures
Hernia repair: [other] or [diaphragmatic]	Repair of diaphragmatic hernia
Hernia, with obstruction	Hernia of abdominal cavity
Hernia: [Richters] or [other specified abdominal cavity NOS]	Richter's femoral hernia
Hernia: [Richters] or [other specified abdominal cavity NOS]	Richter's inguinal hernia
Hernia: [ventral] or [epigastric] or [incisional]	Incisional hernia of anterior abdominal wall (disorder)
Hernia: [ventral] or [epigastric] or [incisional]	Incisional hernia
Hernia: [ventral] or [epigastric] or [incisional]	Hernia of anterior abdominal wall (disorder)
Herpes encephalitis	Encephalitis caused by Herpesvirus
Herpes encephalitis	Encephalitis caused by human herpes simplex virus
Herpes gestationis - delivered	Herpes gestationis
Herpes gestationis - delivered with postnatal complication	Herpes gestationis
Herpes gestationis - not delivered	Herpes gestationis
Herpes gestationis with postnatal complication	Herpes gestationis
Herpes simplex associated with acquired immunodeficiency syndrome	Infection caused by herpes simplex virus co-occurrent with human immunodeficiency virus infection
Herpes simplex encephalitis	Encephalitis caused by human herpes simplex virus
Herpes simplex encephalitis	Encephalitis caused by Herpesvirus
Herpes simplex encephalitis	Meningoencephalitis caused by human herpes simplex virus
Herpes simplex encephalitis	Encephalitis caused by Herpesvirus
Herpes simplex encephalitis	Encephalitis caused by human herpes simplex virus
Herpes simplex group virus	Subfamily Alphaherpesvirinae (organism)
Herpes simplex group virus	Simplexvirus
Herpes simplex septicemia	Sepsis due to herpes simplex (disorder)
Herpes zoster [organism] or [infection - shingles]	Herpes zoster
Herpes zoster [organism] or [infection - shingles]	Varicellovirus humanalpha3 (organism)
Herpes: [gestationis] or [+ pregnancy]	Herpes in pregnancy
Herpes: [gestationis] or [+ pregnancy]	Herpes gestationis
Herpes: [gestationis] or [+ pregnancy]	Herpes gestationis
Herpes: [simplex, no complication NOS] or [labialis]	Herpes labialis
Herpetic gingivostomatitis	Herpes labialis
Herpetic gingivostomatitis	Herpetic gingivostomatitis
Herpetic: [gingivostomatitis] or [cold sore] or [stomatitis]	Herpes labialis

Start Previous Page 224 of 498 Next End

Reference Sets

Reference set descriptor

Description inactivation indicator reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
900000000001150016	POSSIBLY EQUIVALENT TO 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)
900000000001151017	POSSIBLY EQUIVALENT TO association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)