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718183003: Familial thyroid dyshormonogenesis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3311173012 Familial thyroid dyshormonogenesis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3311174018 Familial thyroid dyshormonogenesis en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial thyroid dyshormonogenesis Is a Congenital hypothyroidism true Inferred relationship Existential restriction modifier
Familial thyroid dyshormonogenesis Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
Familial thyroid dyshormonogenesis Occurrence Congenital false Inferred relationship Existential restriction modifier
Familial thyroid dyshormonogenesis Finding site Thyroid structure false Inferred relationship Existential restriction modifier
Familial thyroid dyshormonogenesis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Familial thyroid dyshormonogenesis Finding site Thyroid structure true Inferred relationship Existential restriction modifier 1
Familial thyroid dyshormonogenesis Is a Primary hypothyroidism true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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