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900000000000523009: 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

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
900000000001151017 POSSIBLY EQUIVALENT TO association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component
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
900000000001151017 POSSIBLY EQUIVALENT TO association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component

113178 members. Search Members:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
POSSIBLY EQUIVALENT TO association reference set Is a Historical association reference set (foundation metadata concept) true Inferred relationship Existential restriction modifier (core metadata concept)
Members targetComponentId
[X]Topical hydrocortisone adverse reaction Hydrocortisone adverse reaction (disorder)
[X]Topical hydrocortisone adverse reaction Hydrocortisone adverse reaction
[X]Topical hydrocortisone adverse reaction Hypersensitivity to hydrocortisone
[X]Topical hydrocortisone adverse reaction Hypersensitivity to hydrocortisone
[X]Topical hydrocortisone adverse reaction Hydrocortisone adverse reaction (disorder)
[X]Topical hydrocortisone adverse reaction Allergy to hydrocortisone (finding)
[X]Topical hydrocortisone adverse reaction Hydrocortisone sensitivity
[X]Topical hydrocortisone adverse reaction Allergy to hydrocortisone (finding)
[X]solvents: [mental & behavioural disorders dependence syndrome due to use of] or [drug addiction] Glue sniffing dependence (disorder)
[X]solvents: [mental & behavioural disorders dependence syndrome due to use of] or [drug addiction] Glue sniffing dependence (disorder)
a Tumor staging descriptor a (tumor staging)
a Tumor staging descriptor a (tumor staging)
a.m. peak specimen a.m. peak specimen (qualifier value)
a.m. peak specimen a.m. peak specimen (qualifier value)
beta>2< Glycoprotein Apolipoprotein H (substance)
beta>2< Glycoprotein Apolipoprotein H (substance)
cryotherapy of lesion of palate (procedure) [Ambiguous] Cryotherapy to lesion of palate
cryotherapy of lesion of palate (procedure) [Ambiguous] Cryotherapy to lesion of palate
cryotherapy of lesion of palate (procedure) [Ambiguous] Cryotherapy of palate
cryotherapy of lesion of palate (procedure) [Ambiguous] Cryotherapy of palate
min minute (qualifier value)
min minute (qualifier value)
p Tumor staging descriptor p (tumor staging)
p Tumor staging descriptor p (tumor staging)
p.m. trough specimen p.m. trough specimen (qualifier value)
p.m. trough specimen p.m. trough specimen (qualifier value)
pH observations pH - finding
pH observations pH - finding
pyrilamine maleate+benzocaine Benzocaine- and mepyramine-containing product
pyrilamine maleate+benzocaine Benzocaine- and mepyramine-containing product
r Tumor staging descriptor r (tumor staging)
r Tumor staging descriptor r (tumor staging)
ther specified pulmonary tuberculosis (disorder) Pulmonary tuberculosis (disorder)
ther specified pulmonary tuberculosis (disorder) Respiratory tuberculosis
ther specified pulmonary tuberculosis (disorder) Pulmonary tuberculosis (disorder)
von Hippel internal corneal ulcer Irido-corneo-trabecular dysgenesis (disorder)
von Hippel internal corneal ulcer Irido-corneo-trabecular dysgenesis (disorder)
von Willebrand disease type 2A Von-Willebrand-Syndrom Typ 2A
von Willebrand disease type 2A Hereditary von Willebrand disease type 2A
von Willebrand disease type 2B Hereditary von Willebrand disease type 2B
von Willebrand disease type 2B maladie de von Willebrand type 2B
von Willebrand disease type 2M maladie de von Willebrand type 2M
von Willebrand disease type 2M Hereditary von Willebrand disease type 2M (disorder)
von Willebrand disease type 2N von Willebrand disease Normandy
von Willebrand disease type 2N Hereditary von Willebrand disease type 2N (disorder)
von Willebrand disease type IA von Willebrand disease, type 1^a^
von Willebrand disease type IA Hereditary von Willebrand disease type 1A (disorder)
von Willebrand disease type IA von Willebrand disease type IA
von Willebrand disease, type 1^a^ Hereditary von Willebrand disease type 1A (disorder)
von Willebrand disease, type 1^a^ A form of von Willebrand disease (VWD) with characteristics of a bleeding disorder associated with a partial, quantitative plasmatic deficiency of an otherwise structurally and functionally normal von Willebrand factor (VWF). The type 1 disease is considered to be the most common form of VWD, caused by mutations in the VWF gene (12p13.3). Transmitted in an autosomal dominant manner.
von Willebrand disease, type 1^a^ Hereditary von Willebrand disease type 1A (disorder)
von Willebrand disease, type 1^a^ A form of von Willebrand disease (VWD) with characteristics of a bleeding disorder associated with a partial, quantitative plasmatic deficiency of an otherwise structurally and functionally normal von Willebrand factor (VWF). The type 1 disease is considered to be the most common form of VWD, caused by mutations in the VWF gene (12p13.3). Transmitted in an autosomal dominant manner.
von Willebrand disease, type IIC Hereditary von Willebrand disease
von Willebrand disease, type IIC Hereditary von Willebrand disease type 2
von Willebrand disease, type IIC Hereditary von Willebrand disease type 2
von Willebrand disease, type IIC Hereditary von Willebrand disease
von Willebrand disease, type IID Hereditary von Willebrand disease type 2
von Willebrand disease, type IID Hereditary von Willebrand disease
von Willebrand disease, type IID Hereditary von Willebrand disease type 2
von Willebrand disease, type IID Hereditary von Willebrand disease
von Willebrand disease, type IIE Hereditary von Willebrand disease type 2
von Willebrand disease, type IIE Hereditary von Willebrand disease
von Willebrand disease, type IIE Hereditary von Willebrand disease
von Willebrand disease, type IIE Hereditary von Willebrand disease type 2
von Willebrand disease, type IIF Hereditary von Willebrand disease type 2
von Willebrand disease, type IIF Hereditary von Willebrand disease type 2
von Willebrand disease, type IIF Hereditary von Willebrand disease
von Willebrand disease, type IIF Hereditary von Willebrand disease
von Willebrand disease, type IIG Hereditary von Willebrand disease type 2
von Willebrand disease, type IIG Hereditary von Willebrand disease type 2
von Willebrand disease, type IIG Hereditary von Willebrand disease
von Willebrand disease, type IIG Hereditary von Willebrand disease
von Willebrand disease, type IIH Hereditary von Willebrand disease type 2
von Willebrand disease, type IIH Hereditary von Willebrand disease
von Willebrand disease, type IIH Hereditary von Willebrand disease
von Willebrand disease, type IIH Hereditary von Willebrand disease type 2
y Tumor staging descriptor y (tumor staging)
y Tumor staging descriptor y (tumor staging)

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