65031000119108: Family history of Cowden syndrome (situation)

• SNOMED CT Concept\Situation with explicit context (situation)\...
• \Finding with explicit context (situation)\Family history of clinical finding\Family history of disorder\...
• \Family history of hereditary disease (situation)\Family history of Cowden syndrome (situation)
• \Family history of development disorder\familieanamnese: medfødt misdannelse\Family history of multiple congenital anomalies (situation)\Family history of Cowden syndrome (situation)
• \Family history of development disorder\familieanamnese: medfødt misdannelse\Family history: Congenital gastrointestinal tract anomaly (situation)\Family history of Cowden syndrome (situation)
• \Family history of development disorder\Family history of multiple congenital anomalies (situation)\Family history of Cowden syndrome (situation)
• \Family history of development disorder\Family history: Congenital gastrointestinal tract anomaly (situation)\Family history of Cowden syndrome (situation)
• \Family history of congenital disease (situation)\familieanamnese: medfødt misdannelse\Family history of multiple congenital anomalies (situation)\Family history of Cowden syndrome (situation)
• \Family history of congenital disease (situation)\familieanamnese: medfødt misdannelse\Family history: Congenital gastrointestinal tract anomaly (situation)\Family history of Cowden syndrome (situation)
• \Family history of congenital disease (situation)\Family history of multiple congenital anomalies (situation)\Family history of Cowden syndrome (situation)
• \Family history of congenital disease (situation)\Family history: Congenital gastrointestinal tract anomaly (situation)\Family history of Cowden syndrome (situation)
• \FH: Skin disease\Family history of Cowden syndrome (situation)
• \FH: Gastrointestinal disease\Family history: Congenital gastrointestinal tract anomaly (situation)\Family history of Cowden syndrome (situation)
• \Family history with explicit context (situation)\Family history of clinical finding\Family history of disorder\...
• \Family history of hereditary disease (situation)\Family history of Cowden syndrome (situation)
• \Family history of development disorder\familieanamnese: medfødt misdannelse\Family history of multiple congenital anomalies (situation)\Family history of Cowden syndrome (situation)
• \Family history of development disorder\familieanamnese: medfødt misdannelse\Family history: Congenital gastrointestinal tract anomaly (situation)\Family history of Cowden syndrome (situation)
• \Family history of development disorder\Family history of multiple congenital anomalies (situation)\Family history of Cowden syndrome (situation)
• \Family history of development disorder\Family history: Congenital gastrointestinal tract anomaly (situation)\Family history of Cowden syndrome (situation)
• \Family history of congenital disease (situation)\familieanamnese: medfødt misdannelse\Family history of multiple congenital anomalies (situation)\Family history of Cowden syndrome (situation)
• \Family history of congenital disease (situation)\familieanamnese: medfødt misdannelse\Family history: Congenital gastrointestinal tract anomaly (situation)\Family history of Cowden syndrome (situation)
• \Family history of congenital disease (situation)\Family history of multiple congenital anomalies (situation)\Family history of Cowden syndrome (situation)
• \Family history of congenital disease (situation)\Family history: Congenital gastrointestinal tract anomaly (situation)\Family history of Cowden syndrome (situation)
• \FH: Skin disease\Family history of Cowden syndrome (situation)
• \FH: Gastrointestinal disease\Family history: Congenital gastrointestinal tract anomaly (situation)\Family history of Cowden syndrome (situation)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). 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	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3438377016	Family history of Cowden syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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