723461007: Pierre Robin sequence faciodigital anomaly syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of limb structure\Disorder of extremity\...
• \Disorder of digit\Congenital anomaly of digit\Pierre Robin sequence faciodigital anomaly syndrome
• \Congenital anomaly of limb\Congenital anomaly of digit\Pierre Robin sequence faciodigital anomaly syndrome
• \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\Robin sequence\Pierre Robin sequence faciodigital anomaly syndrome
• \Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Robin sequence\Pierre Robin sequence faciodigital anomaly syndrome
• \Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Robin sequence\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Disorder of extremity\Disorder of digit\Congenital anomaly of digit\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Disorder of extremity\Congenital anomaly of limb\Congenital anomaly of digit\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Robin sequence\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Robin sequence\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Robin sequence\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Robin sequence\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Congenital disease\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Robin sequence\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Robin sequence\Pierre Robin sequence faciodigital anomaly syndrome
• \Disease\Developmental disorder\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit\Pierre Robin sequence faciodigital anomaly syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3424707016	Pierre Robin sequence faciodigital anomaly syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3424708014	Pierre Robin sequence faciodigital anomaly syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3424709018	Chitayat Meunier Hodgkinson syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3424710011	Pierre Robin sequence with facial and digital anomalies	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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