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718194004: Hypothyroidism due to mutation in transcription factor of pituitary development (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
3311456017 Hypothyroidism due to mutation in transcription factor of pituitary development (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3311457014 Hypothyroidism due to mutation in transcription factor of pituitary development 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
Hypothyroidism due to mutation in transcription factor of pituitary development Due to Congenital anomaly of pituitary gland true Inferred relationship Existential restriction modifier 2
Hypothyroidism due to mutation in transcription factor of pituitary development Is a Congenital hypothyroidism true Inferred relationship Existential restriction modifier
Hypothyroidism due to mutation in transcription factor of pituitary development Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
Hypothyroidism due to mutation in transcription factor of pituitary development Occurrence Congenital false Inferred relationship Existential restriction modifier
Hypothyroidism due to mutation in transcription factor of pituitary development Finding site Thyroid structure false Inferred relationship Existential restriction modifier
Hypothyroidism due to mutation in transcription factor of pituitary development Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hypothyroidism due to mutation in transcription factor of pituitary development Finding site Thyroid structure true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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