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
False ragweed pollen allergen	False ragweed pollen
Familial combined hyperlipidemia	Familial combined hyperlipidemia
Familial combined hyperlipidemia	Familial multiple lipoprotein-type hyperlipidaemia
Familial combined hyperlipidemia	Mixed hyperlipidaemia
Familial erythrophagocytic lymphohistiocytosis	Histiocytic medullary reticulosis
Familial erythrophagocytic lymphohistiocytosis	Histiocytic medullary reticulosis
Familial erythrophagocytic lymphohistiocytosis	Familial hemophagocytic lymphohistiocytosis (disorder)
Familial erythrophagocytic lymphohistiocytosis	Familial hemophagocytic lymphohistiocytosis (disorder)
Familial febrile urticaria	Familial amyloid nephropathy with urticaria AND deafness
Familial febrile urticaria	Familial febrile urticaria
Familiær fokal faciodermal dysplasi	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.
Familiær fokal faciodermal dysplasi	Focal facial dermal dysplasias (FFDD) are rare ectodermal dysplasias, with characteristics of congenital bitemporal (resembling forceps marks) or preauricular scar-like lesions associated with additional facial and or systematic manifestations. Four types of FFDD are described. 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. Types I and IV are infrequently associated with extra-cutaneous anomalies.
familiær generaliseret lipodystrofi	Congenital total lipodystrophy (disorder)
Familial generalized lipodystrophy	Congenital total lipodystrophy (disorder)
Familial hemophagocytic lymphohistiocytosis	Familial hemophagocytic lymphohistiocytosis (disorder)
Familial hemophagocytic lymphohistiocytosis	Histiocytic medullary reticulosis
Familial hyperbetalipoproteinaemia	Familial hypercholesterolemia (disorder)
Familial hyperbetalipoproteinaemia	Fredrickson type IIa hyperlipoproteinemia (disorder)
Familial hyperbetalipoproteinaemia	Fredrickson type IIa hyperlipoproteinemia (disorder)
Familial hyperbetalipoproteinaemia	Familial hypercholesterolemia (disorder)
Familial hyperbetalipoproteinaemia	Fredrickson type IIa hyperlipoproteinemia (disorder)
Familial hyperbetalipoproteinaemia	Familial hypercholesterolemia (disorder)
Familial hypercholesterolemia	Familial hypercholesterolemia (disorder)
Familial hypercholesterolemia	Fredrickson type IIa hyperlipoproteinemia (disorder)
Familial hyperparathyroidism	Familial hypocalciuric hypercalcaemia
Familial hyperparathyroidism	Familial hyperparathyroidism
familiær hypokaliæmi-hypomagnesæmi	A rare renal disease characterized by hypokalemic metabolic alkalosis secondary to a tubulopathy, hypomagnesemia with hypermagnesuria, severe hypercalciuria and dilated cardiomyopathy.
familiær hypokaliæmi-hypomagnesæmi	A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. The disease presents mainly in adolescents and adults but also encountered in children, as early as in the neonatal period. Caused by biallelic inactivating mutations in the SLC12A3 gene encoding the thiazide-sensitive sodium-chloride cotransporter NCC expressed in the apical membrane of cells lining the distal convoluted tubule. More than 350 different NCC mutations throughout the whole protein have been identified.
Familial hypokalemic and hypomagnesemic tubulopathy	A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. The disease presents mainly in adolescents and adults but also encountered in children, as early as in the neonatal period. Caused by biallelic inactivating mutations in the SLC12A3 gene encoding the thiazide-sensitive sodium-chloride cotransporter NCC expressed in the apical membrane of cells lining the distal convoluted tubule. More than 350 different NCC mutations throughout the whole protein have been identified.
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 megaloblastic anemia	Selective malabsorption of cyanocobalamin
Familial megaloblastic anemia	Familial megaloblastic anemia
Familiært multitumorsyndrom	Familial neoplastic disease
Familiært multitumorsyndrom	Hereditary cancer-predisposing syndrome
Familial periodic paralysis (& [hypokalaemic])	Familial periodic paralysis
Familial periodic paralysis (& [hypokalaemic])	Familial hypokalemic periodic paralysis
Familial periodic paralysis	Familial periodic paralysis
Familial periodic paralysis	Familial hypokalemic periodic paralysis
Familial periodic paralysis	Periodic paralysis
familiær sea blue-histiocytose	Sea-blue histiocyte syndrome
Familial type 3 hyperlipoproteinemia	Tuberous xanthoma
Familial type 3 hyperlipoproteinemia	Familial type 3 hyperlipoproteinemia (disorder)
Familial type 3 hyperlipoproteinemia	Tubero-eruptive xanthoma (disorder)
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 Rhinolophidae (organism)
Families phyllostomatidae AND/OR hipposideridae	Family Phyllostomidae (organism)
Families tachyglossidae AND/OR ornithorhynchidae	Family Ornithorhynchidae (organism)
Families tachyglossidae AND/OR ornithorhynchidae	Family Tachyglossidae (organism)
Families typhlopidae AND/OR leptotyphlopidae	Family Typhlopidae (organism)
Families typhlopidae AND/OR leptotyphlopidae	Family Leptotyphlopidae (organism)
Families zapodidae AND/OR dipodidae	Family Dipodidae (organism)
Families zapodidae AND/OR dipodidae	Subfamily Zapodinae (organism)
familien Archaeoglobaceae	Family Archaeoglobaceae (organism)
familien Archaeoglobaceae	Order Archaeoglobales (organism)
Familien Dilepidae	Family Dilepididae (organism)
Familien Dilepidae	Family Dipylidiidae
Flexibacteraceae	Family Cytophagaceae (organism)
Flexibacteraceae	Cyclobacteriaceae
Family bereavement	Family bereavement (finding)
Family bereavement	Death of relative
vurdering af familiens sundhedsbehov udført	Assessment of health needs of family done (situation)
gennemgang af vurdering af familiens sundhedsbehov	Assessment of health needs of family (situation)
familieanamnese efter slægtning	Family history with explicit context (situation)
Family history finding	Family history with explicit context (situation)
Family history finding	Family history of clinical finding
familieanamnestisk oplysning	Family history with explicit context (situation)
familieanamnestisk oplysning	Family history of clinical finding
familieanamnese med bronkitis eller kronisk obstruktiv lungesygdom	Family history of bronchitis (situation)
familieanamnese med bronkitis eller kronisk obstruktiv lungesygdom	Family history of chronic obstructive lung disease
Family history of hyperlipoproteinemia a	Family history of Fredrickson type IIa hyperlipoproteinaemia
Family history of hyperlipoproteinemia a	Family history of lipoprotein (a) hyperlipoproteinemia (situation)
Family history of neoplasm of gastrointestinal tract	FH: Stomach cancer
Family history of neoplasm of gastrointestinal tract	FH: Bowel cancer
familieanamnese: karcinom - neoplasme	Family history of malignant epithelial neoplasm (situation)
familieanamnese: karcinom - neoplasme	Family history of neoplasm
familieanamnese: karcinom - neoplasme	Family history of malignant neoplasm
familieanamnese: kolinesterasemangel	Family history of butyrylcholinesterase deficiency
familieanamnese: kolinesterasemangel	Family history of acetylcholinesterase deficiency
familieanamnese: obstetrisk problem	Family history of disorder
familieanamnese: ovariekarcinom	Family history of malignant neoplasm of ovary (situation)
familieanamnese: neoplasme - trachea/bronkie/lunge	Family history of neoplasm of bronchus
familieanamnese: neoplasme - trachea/bronkie/lunge	Family history of neoplasm of trachea
familieanamnese: neoplasme - trachea/bronkie/lunge	Family history of neoplasm of lung
familieanamnese: neoplasme - urinorgan	Family history of malignant neoplasm of urinary tract
familieanamnese: neoplasme - urinorgan	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 history of disability
Family illness (& [relative] or [child]) or handicapped relative	Family illness
Family illness (& [relative] or [child]) or handicapped relative	Sick child
Familen Oestridae - Hypodermatidae	Subfamily Hypodermatinae (organism)
Familen Oestridae - Hypodermatidae	Family Oestridae (organism)
Family paradoxornithidae	Family Sylviidae (organism)
Family paradoxornithidae	Genus Paradoxornis (organism)
Family planning counseling	Family planning education (procedure)

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Reference Sets

Reference set descriptor

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)