6820001000004100: Family history of holoprosencephaly (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 development disorder\Family history of congenital malformation\Family history of multiple congenital anomalies (situation)\Family history of holoprosencephaly (situation)
• \Family history of congenital disease (situation)\Family history of congenital malformation\Family history of multiple congenital anomalies (situation)\Family history of holoprosencephaly (situation)
• \Family history with explicit context (situation)\Family history of clinical finding\Family history of disorder\...
• \Family history of development disorder\Family history of congenital malformation\Family history of multiple congenital anomalies (situation)\Family history of holoprosencephaly (situation)
• \Family history of congenital disease (situation)\Family history of congenital malformation\Family history of multiple congenital anomalies (situation)\Family history of holoprosencephaly (situation)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2015. Module: US National Library of Medicine maintained module (core metadata concept)

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
679391000124114	Family history of holoprosencephaly (situation)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	US National Library of Medicine maintained module (core metadata concept)
679401000124111	Family history of holoprosencephaly	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	US National Library of Medicine maintained module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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