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
Hypertensive renal disease with end stage renal failure	End stage renal disease due to hypertension (disorder)
Hypertensive renal disease with renal failure	Hypertensive renal failure
Hypertensive retinopathy	Hypertensive retinopathy
Hypertensive retinopathy	Arteriosclerotic retinopathy
Hypertensive: [cardiomegaly] or [heart disease NOS without congestive cardiac failure]	Cardiomegaly due to hypertension (disorder)
Hypertensive: [encephalopathy] or [crisis]	Hypertensive encephalopathy
Hyperthermia	Hyperpyrexia (finding)
Hyperthermia-induced defect	A rare maternal disease-related embryofetopathy characterized by variable developmental anomalies of the fetus due to teratogenic effect of elevated maternal body temperature (resulting from febrile illness or hot environment exposure). Reported developmental anomalies include neural tube defects (spina bifida, encephalocele, anencephaly), cardiac defects (transposition of great vessels), urogenital defects (hypospadias), abdominal wall defects, cleft lip/palate, eye defects (cataract, coloboma) or various minor anomalies (e.g., bifid uvula, preauricular pit or tag). Consensus regarding cause-effect relationship has not been reached.
Hypertonic bladder sphincter	Overactive urinary bladder (disorder)
Hypertrophic elongation of cervix	Hypertrophied cervix
Hypertrophic elongation of cervix	Hypertrophic elongation of cervix
Hypertrophic pulmonary osteoarthropathy	Hereditary clubbing (disorder)
Hypertrophic pulmonary osteoarthropathy	Hypertrophic osteoarthropathy
Hypertrophy of clitoris	Hypertrophy of clitoris
Hypertrophy of leg	Hypertrophy of lower leg (finding)
Hypertrophy of leg	Hypertrophy of lower limb
Hypertrophy of thymus	Hypertrophy of thymus
Hypertrophy of uterus	Enlarged uterus
Hypertrophy of uterus	Hypertrophy of uterus
Hypertrophy or dilatation of right ventricle	Dilatation of right cardiac ventricle (disorder)
Hypertrophy or dilatation of right ventricle	Right ventricular hypertrophy
Hyperuricaemia	A disease caused by monosodium urate crystal deposition with any of the following clinical presentations (current or prior): gout flare, chronic gouty arthritis, or subcutaneous tophus.
Hyperuricaemia	Hyperuricemia
Hyphema of iris and ciliary body	Hyphema
Hypnotic AND/OR sedative drug	Hypnotic agent (substance)
Hypnotic AND/OR sedative drug	Sedative (substance)
Hypnotic and/or anxiolytic dependence (& [sedative] or [barbiturate] or [benzodiazepine (& named variants)])	Chlordiazepoxide dependence (disorder)
Hypnotic or anxiolytic	Anxiolytic agent (substance)
Hypnotic or anxiolytic	Hypnotic agent (substance)
Hypocalcemia AND/OR hypomagnesemia of newborn	Neonatal hypomagnesemia
Hypocalcemia AND/OR hypomagnesemia of newborn	Neonatal hypocalcaemia
Hypochoeris species	Hypochoeris (organism)
Hypoderma species	Hypoderma
Hypodermic needle product	Injection device
Hypodermic needle product	Hypodermic needle
Hypodermic needle, reprocessed	Hypodermic needle
Hypodermic needle, single-use, non-sterile	Hypodermic needle
Hypodermic needle, single-use, sterile	Hypodermic needle
Hypodermic needles & syringes	Hypodermic needle
Hypodermic needles & syringes	Syringe
Hypogammaglobulinaemia: [congenital] or [agammaglobulinaemia: (Bruton's) or (congenital sex-linked & [X-linked])]	X-linked agammaglobulinemia
Hypogammaglobulinaemia: [congenital] or [agammaglobulinaemia: (Bruton's) or (congenital sex-linked & [X-linked])]	Congenital hypogammaglobulinaemia
Hypoglossal nerve and its branches	Entire hypoglossal nerve
Hypoglossal nerve and its branches	Hypoglossal nerve structure
Hypoglycaemic coma (& [insulin])	Hypoglycaemic coma
Hypoglycaemic coma	Insulin coma (disorder)
Hypoglycaemic coma (& [insulin])	Insulin coma (disorder)
Hypoglycaemic coma	Hypoglycaemic coma
Hypoglycemia	Hypoglycaemia
Hypoglycemia	Hypoglycaemic syndrome
Hypoglycemic coma	Hypoglycemic shock
Hypoglycemic coma	Hypoglycaemic coma
Hypoglycemic coma in type II diabetes mellitus	Hypoglycemic coma due to type 2 diabetes mellitus
Hypohidrotic ectodermal dysplasia syndrome	Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
Hypohidrotic ectodermal dysplasia syndrome	Hypohidrotic X-linked ectodermal dysplasia
Hypomagnesemia	Hypomagnesaemia
Hypomagnesemia	Hypermagnesaemia
Hypomelanosis of Ito	Incontinentia pigmenti achromians syndrome
Hypomelanosis of Ito	Nevus of Ito
Hypomobility	Limitation of joint movement
Hypomobility	Impaired mobility
Hypophosphatasia	Infantile hypophosphatasia
Hypophosphatasia	Hypophosphatasia
Hypophysectomy: [NOS] or [NEC]	Hypophysectomy
Hypopigmentation of eyelid	Hypopigmentation of eyelid
Hypopigmentation of eyelid	Vitiligo of eyelid
Hypopituit (& [panhypopituitarism])	Panhypopituitarism
Hypopituit (& [panhypopituitarism])	Panhypopituitarism
Hypopituit (& [panhypopituitarism])	Hypopituitarism
Hypopituitarism: [NOS] or [Sheehan's syndrome] or [Simmond's disease] or [Panhypopituitarism]	Panhypopituitarism
Hypopituitarism: [NOS] or [Sheehan's syndrome] or [Simmond's disease] or [Panhypopituitarism]	Sheehan's syndrome (disorder)
Hypoplasia of aorta (& [tubular])	Tubular hypoplasia of aorta
Hypoplasia of aorta (& [tubular])	Hypoplasia of aorta
Hypoplasia of bone marrow	Hypocellular bone marrow (finding)
Hypoplasia of bone marrow	Bone marrow depression
Hypoplasia of brain, part unspecified	Congenital brain aplasia (disorder)
Hypoplasia of part of brain NEC	Congenital brain aplasia (disorder)
Hypoplasia of thyroid	Hypoplasia of thyroid (disorder)
Hypoplasia of thyroid	Thyroid atrophy
Hypoplasmic obesity	Obesity (disorder)
Hyposmolality &/or hyponatraemia	Hypo-osmolality and or hyponatremia
Hyposmolality &/or hyponatraemia	Hyponatremia
Hyposmolality	Hyposmolality
Hyposmolality	Hypotonic disorder
Hyposmolality	Hyposmolality syndrome
Hypospadias &/or epispadias	Epispadias (disorder)
Hypospadias &/or epispadias	Hypospadias (disorder)
Hypospadias &/or epispadias	Epispadias (disorder)
Hypospadias &/or epispadias	Hypospadias (disorder)
Hypospadias &/or epispadias	Male epispadias (disorder)
Hypospadias	Epispadias (disorder)
Hypospadias	Hypospadias (disorder)
Hypospadias	Hypospadias (disorder)
Hypospadias	Epispadias (disorder)
Hypospadias and chordee repair	Denis-Browne hypospadias repair
Hypospadias and chordee repair	Hypospadias and chordee repair (procedure)
Hypospadias and epispadias	Epispadias (disorder)
Hypospadias and epispadias	Hypospadias (disorder)
Hypospadias or epispadias NOS	Epispadias (disorder)
Hypospadias or epispadias NOS	Hypospadias (disorder)
Hypospadias repair	Female hypospadias repair

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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)