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237517001: Congenital atrophy of thyroid (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
355960013 Congenital atrophy of thyroid en Synonym Active Entire term case insensitive SNOMED CT core module
626258016 Congenital atrophy of thyroid (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital atrophy of thyroid Is a Congenital hypothyroidism without goiter false Inferred relationship Existential restriction modifier
Congenital atrophy of thyroid Is a Congenital anomaly of the thyroid gland false Inferred relationship Existential restriction modifier
Congenital atrophy of thyroid Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital atrophy of thyroid Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Congenital atrophy of thyroid Finding site Thyroid structure false Inferred relationship Existential restriction modifier 1
Congenital atrophy of thyroid Associated etiologic finding Iodine deficiency false Inferred relationship Existential restriction modifier
Congenital atrophy of thyroid Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
Congenital atrophy of thyroid Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Congenital atrophy of thyroid Is a Thyroid atrophy true Inferred relationship Existential restriction modifier
Congenital atrophy of thyroid Associated morphology Congenital atrophy false Inferred relationship Existential restriction modifier 1
Congenital atrophy of thyroid Associated morphology Congenital atrophy false Inferred relationship Existential restriction modifier 1
Congenital atrophy of thyroid Finding site Thyroid structure false Inferred relationship Existential restriction modifier 1
Congenital atrophy of thyroid Is a Congenital disease true Inferred relationship Existential restriction modifier
Congenital atrophy of thyroid Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital atrophy of thyroid Associated morphology Atrophy true Inferred relationship Existential restriction modifier 2
Congenital atrophy of thyroid Finding site Thyroid structure true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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