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1179394003: Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4651001014 Congenital hypothyroidism due to thyroid peroxidase mutation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4651002019 Congenital hypothyroidism due to thyroid peroxidase mutation en Synonym (core metadata concept) 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
Congenital hypothyroidism due to thyroid peroxidase mutation (disorder) est un(e) (attribut) Congenital hypothyroidism true Inferred relationship Some
Congenital hypothyroidism due to thyroid peroxidase mutation (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Congenital hypothyroidism due to thyroid peroxidase mutation (disorder) localisation d'une constatation (attribut) structure de la thyroïde true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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