65031000119108: Family history of Cowden syndrome (situation)

• SNOMED CT Concept\Situation with explicit context\...
• \Finding with explicit context\Family history of clinical finding\Family history of disorder\...
• \Family history of hereditary disease\Family history of Cowden syndrome
• \Family history of development disorder\Family history of multiple congenital anomalies\Family history of Cowden syndrome
• \Family history of development disorder\FH: Congenital GIT anomaly\Family history of Cowden syndrome
• \Family history of congenital disease\Family history of multiple congenital anomalies\Family history of Cowden syndrome
• \Family history of congenital disease\FH: Congenital GIT anomaly\Family history of Cowden syndrome
• \FH: Skin disease\Family history of Cowden syndrome
• \FH: Gastrointestinal disease\FH: Congenital GIT anomaly\Family history of Cowden syndrome
• \Family history with explicit context\Family history of clinical finding\Family history of disorder\...
• \Family history of hereditary disease\Family history of Cowden syndrome
• \Family history of development disorder\Family history of multiple congenital anomalies\Family history of Cowden syndrome
• \Family history of development disorder\FH: Congenital GIT anomaly\Family history of Cowden syndrome
• \Family history of congenital disease\Family history of multiple congenital anomalies\Family history of Cowden syndrome
• \Family history of congenital disease\FH: Congenital GIT anomaly\Family history of Cowden syndrome
• \FH: Skin disease\Family history of Cowden syndrome
• \FH: Gastrointestinal disease\FH: Congenital GIT anomaly\Family history of Cowden syndrome

Status: current, Defined. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3438376013	Family history of Cowden syndrome (situation)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3438377016	Family history of Cowden syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Situation with explicit context foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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