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900000000000526001: REPLACED BY association reference set (foundation metadata concept)


Status: current, Necessary but not sufficient concept 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 Reference Sets
900000000001156010 REPLACED BY 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) GB English: Preferred (foundation metadata concept)
900000000001157018 REPLACED BY association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept) GB English: Preferred (foundation metadata concept)

5809 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
REPLACED BY association reference set (foundation metadata concept) Is a Historical association reference set (foundation metadata concept) true Inferred relationship Some

Members targetComponentId
pN0(mol-): No regional lymph node metastasis histologically, negative molecular findings (breast) pN0(mol-): No regional lymph node metastasis histologically, negative nonmorphologic (molecular) findings for isolated tumor cells (breast) (finding)
pT4a: Tumor directly invades other organs or structures (colon/rectum) pT4a: Tumor penetrates to surface of visceral peritoneum (colon/rectum) (finding)
pT4b: Tumor involves masticator space, pterygoid plates, or skull base and/or encases internal carotid artery (oropharynx) pT4b: Tumor invades lateral pterygoid muscle, pterygoid plates, lateral nasopharynx, or skull base or encases internal carotid artery (oropharynx) (finding)
pT4b: Tumor penetrates visceral peritoneum (colon/rectum) pT4b: Tumor directly invades or is adherent to other organs or structures (colon/rectum) (finding)
para-aminohippuric acid Para-aminohippuric acid
r phenotype cde haplotype (finding)
r'' phenotype cdE haplotype (finding)
ry phenotype CdE haplotype (finding)
von Willebrand disease von Willebrand disorder

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Reference Sets

Reference set descriptor

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