64851000119105: Family history of Prader-Willi 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 development disorder\Family history of congenital malformation\Family history of multiple congenital anomalies (situation)\Family history of Prader-Willi syndrome
• \Family history of neurological disorder\FH: CNS disorder\FH: Brain disorder\Family history of Prader-Willi syndrome
• \FH: Genitourinary disease\Family history of Prader-Willi syndrome
• \Family history of congenital disease (situation)\Family history of congenital malformation\Family history of multiple congenital anomalies (situation)\Family history of Prader-Willi syndrome
• \Family history of endocrine disorders (situation)\Family history of Prader-Willi syndrome
• \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 Prader-Willi syndrome
• \Family history of neurological disorder\FH: CNS disorder\FH: Brain disorder\Family history of Prader-Willi syndrome
• \FH: Genitourinary disease\Family history of Prader-Willi syndrome
• \Family history of congenital disease (situation)\Family history of congenital malformation\Family history of multiple congenital anomalies (situation)\Family history of Prader-Willi syndrome
• \Family history of endocrine disorders (situation)\Family history of Prader-Willi syndrome

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3043730013	Family history of Prader-Willi syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3043751011	Family history of Prader-Willi syndrome (situation)	en	Fully specified name	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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