1251449006: Ubiquitin specific peptidase 18 deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Central nervous system finding\Finding of brain\Encephalopathy\Degenerative brain disorder\USP18 deficiency
• \Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Degenerative brain disorder\USP18 deficiency
• \Central nervous system finding\Disorder of the central nervous system\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\USP18 deficiency
• \Central nervous system finding\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\USP18 deficiency
• \Finding of head and neck region\Head finding\...
• \Finding of head circumference\Microcephaly\USP18 deficiency
• \Finding of brain\Encephalopathy\Degenerative brain disorder\USP18 deficiency
• \Disorder of head\Encephalopathy\Degenerative brain disorder\USP18 deficiency
• \General finding of observation of patient\Body measurement finding\Finding of head circumference\Microcephaly\USP18 deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\USP18 deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\USP18 deficiency
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\USP18 deficiency
• \Disease\Disorder of immune function\Autoinflammatory disease\USP18 deficiency
• \Disease\Disorder of immune function\Hereditary disorder of immune system\USP18 deficiency
• \Disease\Degenerative disorder\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\USP18 deficiency
• \Disease\Degenerative disorder\Degenerative disease of the central nervous system\Degenerative brain disorder\USP18 deficiency
• \Disease\Disorder of body system\Disorder of immune structure\Inflammatory disorder of immune system\Autoinflammatory disease\USP18 deficiency
• \Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of immune system\Autoinflammatory disease\USP18 deficiency
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\USP18 deficiency
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\USP18 deficiency
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\USP18 deficiency
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Degenerative brain disorder\USP18 deficiency
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\USP18 deficiency
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\USP18 deficiency
• \Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of immune system\Autoinflammatory disease\USP18 deficiency
• \Disease\Disorder of head\Encephalopathy\Degenerative brain disorder\USP18 deficiency

Status: current, Primitive. Date: 30-Sep 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5133517011	Ubiquitin specific peptidase 18 deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
5133518018	USP18 deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
5133519014	Ubiquitin specific peptidase 18 deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
5133520015	A rare genetic neurological disorder characterized by severe pseudo-TORCH syndrome with signs of brain damage and occasionally systemic manifestations resembling the sequelae of congenital infection, but in the absence of an infectious agent. Characteristic features include microcephaly, white matter disease, cerebral atrophy, cerebral hemorrhage and calcifications among others. Affected individuals typically have seizures and respiratory insufficiency and die in infancy.	en	Definition	Active	Case sensitive	SNOMED CT core
5133521016	A rare genetic neurological disorder characterised by severe pseudo-TORCH syndrome with signs of brain damage and occasionally systemic manifestations resembling the sequelae of congenital infection, but in the absence of an infectious agent. Characteristic features include microcephaly, white matter disease, cerebral atrophy, cerebral haemorrhage and calcifications among others. Affected individuals typically have seizures and respiratory insufficiency and die in infancy.	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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