OMOP Concept 376106
Disorder of the central nervous system
StandardConditionSNOMED23853001Disorder
Maps from
48
Descendants
9,258
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
48 source codes normalize to Disorder of the central nervous system via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Disorder of the central nervous system across source vocabularies.
- Central nervous system (CNS) disease
- Disorder of the central nervous system (disorder)
- Encephalomyeloneuropathy
- enfermedad del sistema nervioso central
- trastorno del sistema nervioso central
- trastorno del sistema nervioso central (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(5)Roll up to these when you need a wider cohort.
Narrower concepts
(9,258)Included automatically when you query with descendants.
- 12-methyl-3-hydroxybutyric aciduria
- 13-phosphoglycerate dehydrogenase deficiency juvenile form
- 1Acute focal hypoxic neuronal necrosis
- 1Axonal neuropathy
- 1Bruns nystagmus
- 1Central nervous system complication
- 1Central nervous system complication of anesthesia during the puerperium
- 1Central nervous system depression
- 1Central nervous system dysfunction in newborn
- 1Central pain syndrome
- 1Cerebrospinal fluid circulation disorder
- 1Cerebrospinal fluid leak
- 1Cerebrovascular and spinal vascular disorders
- 1Congenital anomaly of central nervous system
- 1Congenital spastic foot
- 1Cyst of central nervous system
- 1Deficiency of alpha-ketoglutarate dehydrogenase
- 1Degenerative disease of the central nervous system
- 1Disorder of brain
- 1Disorder of central nervous system co-occurrent with human immunodeficiency virus infection
- 1Disorder of central nervous system due to and following procedure
- 1Disorder of meninges
- 1Disorder of visual pathways
- 1Epidural abscess
- 1Epidural lipomatosis
- 1Functional disease of the CNS with neuroendocrine disturbance
- 1Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome
- 1Hemiparesis
- 1Hemiplegia
- 1Hemorrhage into extradural space of neuraxis
- 1Hemorrhage into subpial space of neuraxis
- 1Hereditary cerebral hemorrhage with amyloidosis
- 1Hereditary neuraxial edema
- 1Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
- 1Infectious disease of central nervous system
- 1Inflammatory disease of the central nervous system
- 1Injury of central nervous system
- 1Intracranial hypotension
- 1Lipoic acid synthetase deficiency
- 1Malformation of central nervous system of fetus
- 1Mitochondrial respiratory chain complex I assembly gene defect
- 1Mitochondrial respiratory chain complex I structural subunit gene defect
- 1Neoplasm of central nervous system
- 1Obstetric anesthesia with central nervous system complications
- 1PPM-X syndrome
- 1PRUNE1-related neurological syndrome
- 1Spastic ataxia with congenital miosis
- 1Spastic syndrome
- 1Spinal cord disease
- 1Superficial siderosis of central nervous system
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