30915001: Holoprosencephaly sequence (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of head and neck region\Head finding\Disorder of head\Congenital anomaly of head\Holoprosencephaly sequence
• \Disease\Disorder of head\Congenital anomaly of head\Holoprosencephaly sequence
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Malformation sequence\Holoprosencephaly sequence
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of head\Holoprosencephaly sequence
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Malformation sequence\Holoprosencephaly sequence
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of head\Holoprosencephaly sequence

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
484738017	HPE - Holoprosencephaly	en	Synonym	Active	Case sensitive	SNOMED CT core
51765017	Holoprosencephaly sequence	en	Synonym	Active	Case insensitive	SNOMED CT core
51766016	Holoprosencephaly	en	Synonym	Active	Case insensitive	SNOMED CT core
51768015	Familial alobar holoprosencephaly	en	Synonym	Active	Case insensitive	SNOMED CT core
761977010	Holoprosencephaly sequence (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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