1220594007: Pierpont syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Mental state, behaviour and/or psychosocial function finding\Behaviour finding\Intellectual disability\Pierpont syndrome
• \Finding of limb structure\Disorder of extremity\Disorder of lower limb\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 limb\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\Intellectual ability - finding\Intellectual disability\Pierpont syndrome
• \Functional finding\Intelligence finding\Intellectual ability - finding\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 limb\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 anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Pierpont syndrome
• \Disease\Congenital disease\Congenital anomaly\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 anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Pierpont syndrome
• \Disease\Developmental disorder\Congenital anomaly\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, Primitive. Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5045329017	Plantar lipomatosis, facial dysmorphism, developmental delay syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
5045330010	Pierpont syndrome (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
5045331014	Pierpont syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
5045332019	A rare multiple congenital anomalies/dysmorphic syndrome with characteristics of axial hypotonia after birth, prolonged feeding difficulties, moderate to severe global developmental delay, seizures (in particular absence seizures), fetal digital pads, distinctive plantar fat pads anteromedial to the heels, and deep palmar and plantar grooves. Over time, fat pads may become less prominent and disappear. Distinct craniofacial dysmorphic features include a broad face with high forehead, high anterior hairline, narrow palpebral fissures that take on a crescent moon shape when smiling, broad nasal bridge and tip with anteverted nostrils, mild midfacial hypoplasia, long smooth philtrum, thin upper lip vermillion, small, widely spaced teeth, and flat occiput/microcephaly/brachycephaly.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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