1167371007: Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Mental state, behaviour and/or psychosocial function finding\Behaviour finding\Intellectual disability\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Central nervous system finding\Finding of brain\Seizure\Seizure disorder\Epilepsy\Refractory epilepsy\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Central nervous system finding\Finding of brain\Encephalopathy\Seizure disorder\Epilepsy\Refractory epilepsy\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Seizure disorder\Epilepsy\Refractory epilepsy\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Finding of head and neck region\Head finding\...
• \Finding of brain\Seizure\Seizure disorder\Epilepsy\Refractory epilepsy\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Finding of brain\Encephalopathy\Seizure disorder\Epilepsy\Refractory epilepsy\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Finding of head region\Finding of face\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disorder of head\Encephalopathy\Seizure disorder\Epilepsy\Refractory epilepsy\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Functional finding\Cognitive function finding\Intellectual ability - finding\Intellectual disability\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Functional finding\Intelligence finding\Intellectual ability - finding\Intellectual disability\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Neurological finding\Seizure related finding\Seizure\Seizure disorder\Epilepsy\Refractory epilepsy\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Seizure disorder\Epilepsy\Refractory epilepsy\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Disorder of head\Disorder of face\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Disorder of head\Encephalopathy\Seizure disorder\Epilepsy\Refractory epilepsy\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with facial defects as major feature\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of head\Congenital anomaly of face\Multiple malformation syndrome with facial defects as major feature\Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome

Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4603870014	Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4603871013	PMSE (polyhydramnios, megalencephaly, symptomatic epilepsy) syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
4603872018	Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
4603873011	A rare genetic neurological disorder with characteristics of pregnancy complicated by polyhydramnios, severe intractable epilepsy presenting in infancy, severe hypotonia, decreased muscle mass, global developmental delay, craniofacial dysmorphism (long face, large forehead, peaked eyebrows, broad nasal bridge, hypertelorism, large mouth with thick lips), and macrocephaly due to megalencephaly and hydrocephalus in most patients. Additional features that have been reported include cardiac anomalies like atrial septal defects, diabetes insipidus and nephrocalcinosis among others.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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