71271000119107: Family history of retinitis pigmentosa (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 retinitis pigmentosa (situation)
• \FH: Eye disorder\Family history of non-glaucomatous eye disorder (situation)\Family history of retinitis pigmentosa (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 retinitis pigmentosa (situation)
• \FH: Eye disorder\Family history of non-glaucomatous eye disorder (situation)\Family history of retinitis pigmentosa (situation)

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2989890016	Family history of retinitis pigmentosa (situation)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2990264016	Family history of retinitis pigmentosa	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3686661000052110	hereditet för retinitis pigmentosa	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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