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
Fallopian tube repair	Tuboplasty for sterilization reversal (procedure)
Fallopian tube repair	Reversal of female sterilization (procedure)
Fallopian tube repair	Tuboplasty for sterilization reversal (procedure)
Fallopian tube repair	Tubotubal anastomosis (procedure)
Fallopian tube repair	Oophorostomy
Fallopian tube repair	Reversal of female sterilization (procedure)
False ragweed pollen allergen	False ragweed pollen
Familial combined hyperlipidemia	Mixed hyperlipidaemia
Familial combined hyperlipidemia	Familial multiple lipoprotein-type hyperlipidemia
Familial combined hyperlipidemia	Familial combined hyperlipidemia
Familial erythrophagocytic lymphohistiocytosis	Omenn syndrome (OS) is an inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency.
Familial erythrophagocytic lymphohistiocytosis	Familial hemophagocytic lymphohistiocytosis (disorder)
Familial erythrophagocytic lymphohistiocytosis	Familial hemophagocytic lymphohistiocytosis (disorder)
Familial erythrophagocytic lymphohistiocytosis	Omenn syndrome (OS) is an inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency.
Familial febrile urticaria	Familial febrile urticaria
Familial febrile urticaria	Familial amyloid nephropathy with urticaria AND deafness
Familial focal facial dermal dysplasia	Focal facial dermal dysplasia type I (FFDD1), also known as Brauer syndrome, is a focal facial dysplasia with characteristics of congenital bitemporal cutis aplasia. The bitemporal rarely unilateral hypoplastic scar-like lesions in FFDD, resembling forceps marks, are usually the only manifestations of FFDD1. Most patients usually have normal intelligence. Transmitted in an autosomal dominant manner with full penetrance.
Familial focal facial dermal dysplasia	Focal facial dermal dysplasias (FFDD) are rare ectodermal dysplasias, characterized by congenital bitemporal (resembling forceps marks) or preauricular scar-like lesions associated with additional facial and or systematic manifestations. 4 types of FFDD are described. FFDD types II and III present with a variable facial dysmorphism including distichiasis (upper lashes) or lacking eyelashes, and upward slanting and thinned lateral eyebrows with a flattened nasal bridge and full upper lip. FFDD types I and IV are infrequently associated with extra-cutaneous anomalies.
Familial generalized lipodystrophy	Congenital total lipodystrophy (disorder)
Familial generalized lipodystrophy	Congenital total lipodystrophy (disorder)
Familial hemophagocytic lymphohistiocytosis	Omenn syndrome (OS) is an inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency.
Familial hemophagocytic lymphohistiocytosis	Familial hemophagocytic lymphohistiocytosis (disorder)
Familial hyperbetalipoproteinaemia	Familial hypercholesterolemia (disorder)
Familial hyperbetalipoproteinaemia	Familial hypercholesterolemia (disorder)
Familial hyperbetalipoproteinaemia	Familial hypercholesterolemia (disorder)
Familial hyperbetalipoproteinaemia	Fredrickson type IIa hyperlipoproteinemia (disorder)
Familial hyperbetalipoproteinaemia	Fredrickson type IIa hyperlipoproteinemia (disorder)
Familial hyperbetalipoproteinaemia	Fredrickson type IIa hyperlipoproteinemia (disorder)
Familial hypercholesterolemia	Fredrickson type IIa hyperlipoproteinemia (disorder)
Familial hypercholesterolemia	Familial hypercholesterolemia (disorder)
Familial hyperparathyroidism	Familial hypocalciuric hypercalcaemia
Familial hyperparathyroidism	Familial hyperparathyroidism
Familial hypokalemia-hypomagnesemia	A rare renal disease characterized by hypokalemic metabolic alkalosis secondary to a tubulopathy, hypomagnesemia with hypermagnesuria, severe hypercalciuria and dilated cardiomyopathy.
Familial hypokalemia-hypomagnesemia	A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion.
Familial hypokalemic and hypomagnesemic tubulopathy	A rare renal disease characterized by hypokalemic metabolic alkalosis secondary to a tubulopathy, hypomagnesemia with hypermagnesuria, severe hypercalciuria and dilated cardiomyopathy.
Familial hypokalemic and hypomagnesemic tubulopathy	A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion.
Familial megaloblastic anemia	Selective malabsorption of cyanocobalamin
Familial megaloblastic anemia	Familial megaloblastic anemia
Familial multiple tumor syndrome	Hereditary cancer-predisposing syndrome
Familial multiple tumor syndrome	Familial neoplastic disease
Familial periodic paralysis (& [hypokalaemic])	Familial hypokalemic periodic paralysis
Familial periodic paralysis (& [hypokalaemic])	Familial periodic paralysis
Familial periodic paralysis	Familial hypokalemic periodic paralysis
Familial periodic paralysis	Periodic paralysis
Familial periodic paralysis	Familial periodic paralysis
Familial sea-blue histiocytosis	Sea-blue histiocyte syndrome
Familial type 3 hyperlipoproteinemia	Tubero-eruptive xanthoma (disorder)
Familial type 3 hyperlipoproteinemia	Familial type 3 hyperlipoproteinemia (disorder)
Familial type 3 hyperlipoproteinemia	Tuberous xanthoma
Families casuariidae AND/OR dromiceidae	Family Dromaiidae (organism)
Families casuariidae AND/OR dromiceidae	Family Casuariidae (organism)
Families dinomyidae AND/OR dasyproctidae	Subfamily Dasyproctinae (organism)
Families dinomyidae AND/OR dasyproctidae	Family Dinomyidae (organism)
Families heteromyidae AND/OR geomyidae	Family Heteromyidae (organism)
Families heteromyidae AND/OR geomyidae	Family Geomyidae (organism)
Families hystricidae AND/OR erithizontidae	Family Erethizontidae (organism)
Families hystricidae AND/OR erithizontidae	Family Hystricidae (organism)
Families phyllostomatidae AND/OR hipposideridae	Family Phyllostomidae (organism)
Families phyllostomatidae AND/OR hipposideridae	Family Rhinolophidae (organism)
Families tachyglossidae AND/OR ornithorhynchidae	Family Tachyglossidae (organism)
Families tachyglossidae AND/OR ornithorhynchidae	Family Ornithorhynchidae (organism)
Families typhlopidae AND/OR leptotyphlopidae	Family Typhlopidae (organism)
Families typhlopidae AND/OR leptotyphlopidae	Family Leptotyphlopidae (organism)
Families zapodidae AND/OR dipodidae	Subfamily Zapodinae (organism)
Families zapodidae AND/OR dipodidae	Family Dipodidae (organism)
Family Archaeoglobales	Order Archaeoglobales (organism)
Family Archaeoglobales	Family Archaeoglobaceae (organism)
Family Dilepidae - dipylidiidae	Family Dipylidiidae
Family Dilepidae - dipylidiidae	Family Dilepididae (organism)
Family Flexibacteraceae	Family Cytophagaceae (organism)
Family Flexibacteraceae	Cyclobacteriaceae
Family bereavement	Family bereavement (finding)
Family bereavement	Death of relative
Family health needs assessment done	Assessment of health needs of family done (situation)
Family health needs assessment review	Assessment of health needs of family (situation)
Family history by relative	Family history with explicit context (situation)
Family history finding	Family history with explicit context (situation)
Family history finding	Family history of clinical finding
Family history observation	Family history of clinical finding
Family history observation	Family history with explicit context (situation)
Family history of bronchitis or chronic obstructive airway disease	Family history of chronic obstructive lung disease
Family history of bronchitis or chronic obstructive airway disease	Family history of bronchitis (situation)
Family history of hyperlipoproteinemia a	Family history of lipoprotein (a) hyperlipoproteinemia (situation)
Family history of hyperlipoproteinemia a	Family history of Fredrickson type IIa hyperlipoproteinaemia
Family history of neoplasm of gastrointestinal tract	FH: Bowel cancer
Family history of neoplasm of gastrointestinal tract	FH: Stomach cancer
Family history: Carcinoma - Neoplasm	Family history of neoplasm
Family history: Carcinoma - Neoplasm	Family history of malignant neoplasm
Family history: Carcinoma - Neoplasm	Family history of malignant epithelial neoplasm (situation)
Family history: Cholinesterase deficiency	Family history of butyrylcholinesterase deficiency
Family history: Cholinesterase deficiency	Family history of acetylcholinesterase deficiency
Family history: Obstetric problem	Family history of disorder
Family history: Ovarian carcinoma	Family history of malignant neoplasm of ovary (situation)
Family history: neoplasm - trachea/bronchus/lung	Family history of neoplasm of trachea
Family history: neoplasm - trachea/bronchus/lung	Family history of neoplasm of bronchus
Family history: neoplasm - trachea/bronchus/lung	Family history of neoplasm of lung
Family history: neoplasm - urinary organ	Family history of malignant neoplasm of urinary tract
Family history: neoplasm - urinary organ	Family history of neoplasm of urinary system (situation)
Family history: neoplasm of ears, nose, throat	Family history of neoplasm of upper aerodigestive tract (situation)
Family illness (& [relative] or [child]) or handicapped relative	Family illness
Family illness (& [relative] or [child]) or handicapped relative	Sick child

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Reference Sets

Reference set descriptor

Description inactivation indicator reference set

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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)