439143004: Simpson-Golabi-Behmel syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of head and neck region\Head finding\...
• \Finding of head region\Finding of face\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Simpson-Golabi-Behmel syndrome
• \Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Simpson-Golabi-Behmel syndrome
• \Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Simpson-Golabi-Behmel syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary neoplastic syndrome\Simpson-Golabi-Behmel syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Simpson-Golabi-Behmel syndrome
• \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\Simpson-Golabi-Behmel syndrome
• \Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Simpson-Golabi-Behmel syndrome
• \Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Simpson-Golabi-Behmel syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Simpson-Golabi-Behmel syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with early overgrowth\Simpson-Golabi-Behmel syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Simpson-Golabi-Behmel syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Simpson-Golabi-Behmel syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Simpson-Golabi-Behmel syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with early overgrowth\Simpson-Golabi-Behmel syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Simpson-Golabi-Behmel syndrome

Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2789362014	Simpson-Golabi-Behmel syndrome (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
2791857019	Bulldog syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
2794097016	Simpson-Golabi-Behmel syndrome	en	Synonym	Active	Case sensitive	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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