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28047004: Embryonal carcinoma (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
46954010 Embryonal carcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46956012 Embryonal adenocarcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
758683016 Embryonal carcinoma (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
46954010 Embryonal carcinoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
46954010 Embryonal carcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
46956012 Embryonal adenocarcinoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
46956012 Embryonal adenocarcinoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
758683016 Embryonal carcinoma (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
758683016 Embryonal carcinoma (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Embryonal carcinoma (morphologic abnormality) Is a Germ cell neoplasm (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)
Embryonal carcinoma (morphologic abnormality) Is a Malignant neoplasm, primary false Inferred relationship Existential restriction modifier (core metadata concept)
Embryonal carcinoma (morphologic abnormality) Is a Malignant germ cell neoplasm (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
[M]Embryonal carcinoma NOS Is a False Embryonal carcinoma (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Embryonal carcinoma of ovary (disorder) Associated morphology False Embryonal carcinoma (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Embryonal carcinoma of ovary (disorder) Associated morphology True Embryonal carcinoma (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary embryonal carcinoma of testis Associated morphology False Embryonal carcinoma (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Embryonal carcinoma Associated morphology True Embryonal carcinoma (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary embryonal carcinoma of liver Associated morphology True Embryonal carcinoma (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary embryonal carcinoma of brain (disorder) Associated morphology True Embryonal carcinoma (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary embryonal carcinoma of testis Associated morphology True Embryonal carcinoma (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Percent of embryonal carcinoma in primary malignant mixed germ cell tumour of testis Component True Embryonal carcinoma (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1

This concept is not in any reference sets

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