1220594007: Pierpont syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Mental state, behavior and/or psychosocial function finding\Behavior finding\Intellectual disability\Pierpont syndrome
• \Finding of limb structure\Disorder of extremity\Disorder of lower extremity\Disorder of free lower limb\Disorder of foot\Pierpont syndrome
• \Finding of limb structure\Finding of lower limb\Finding of ankle or foot\Finding of foot region\Disorder of foot\Pierpont syndrome
• \Finding of limb structure\Finding of lower limb\Disorder of lower extremity\Disorder of free lower limb\Disorder of foot\Pierpont 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\Pierpont syndrome
• \Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Pierpont syndrome
• \Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Pierpont syndrome
• \Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\Pierpont syndrome
• \Functional finding\Cognitive function finding\Finding of intellectual ability\Intellectual disability\Pierpont syndrome
• \Functional finding\Intelligence finding\Finding of intellectual ability\Intellectual disability\Pierpont syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Pierpont syndrome
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Pierpont syndrome
• \Disease\Lipomatosis\Pierpont syndrome
• \Disease\Disorder of extremity\Disorder of lower extremity\Disorder of free lower limb\Disorder of foot\Pierpont syndrome
• \Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Pierpont syndrome
• \Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Pierpont syndrome
• \Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Pierpont syndrome
• \Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Pierpont syndrome
• \Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\Pierpont syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Pierpont syndrome
• \Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Pierpont syndrome
• \Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Pierpont syndrome
• \Disease\Developmental disorder\Developmental delay\Global developmental delay\Pierpont syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-May 2022. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5045329017	Plantar lipomatosis, facial dysmorphism, developmental delay syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
5045330010	Pierpont syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
5045331014	Pierpont syndrome	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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