63931000119106: Family history of Steinert myotonic dystrophy (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 Steinert myotonic dystrophy
• \Family history of development disorder\FH: Muscular dystrophy\Family history of Steinert myotonic dystrophy
• \Family history of chronic medical disorder\FH: Muscular dystrophy\Family history of Steinert myotonic dystrophy
• \FH: Musculoskeletal disease\FH: Muscular dystrophy\Family history of Steinert myotonic dystrophy
• \Family history with explicit context\Family history of clinical finding\Family history of disorder\...
• \Family history of hereditary disease\Family history of Steinert myotonic dystrophy
• \Family history of development disorder\FH: Muscular dystrophy\Family history of Steinert myotonic dystrophy
• \Family history of chronic medical disorder\FH: Muscular dystrophy\Family history of Steinert myotonic dystrophy
• \FH: Musculoskeletal disease\FH: Muscular dystrophy\Family history of Steinert myotonic dystrophy

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3467660017	Family history of Steinert myotonic dystrophy (situation)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3467661018	Family history of Steinert myotonic dystrophy	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3467662013	Family history of myotonic muscular dystrophy	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Situation with explicit context foundation reference set

Problem/Diagnosis reference set

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