OMOP Concept 374142
Congenital anomaly of nervous system
StandardConditionSNOMED88425004Disorder
Maps from
46
Descendants
611
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
46 source codes normalize to Congenital anomaly of nervous system via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Congenital anomaly of nervous system across source vocabularies.
- anomalía congénita del sistema nervioso
- anomalía congénita del sistema nervioso (trastorno)
- Congenital anomaly of nervous system (disorder)
- Congenital deformity of nervous system
- Congenital disease of nervous system
- Congenital lesion of nervous system
- Congenital malformation of the nervous system
- deformidad congénita del sistema nervioso
- malformación congénita del sistema nervioso
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
Narrower concepts
(611)Included automatically when you query with descendants.
- 1Abnormality of neurogenesis
- 1Agenesis of nerve
- 1Angelman syndrome
- 1Cerebro-oculo-facio-skeletal syndrome
- 1Congenital anomaly of central nervous system
- 1Congenital anomaly of nervous system of head/neck
- 1Congenital anomaly of neural structure of trunk
- 1Congenital anomaly of the peripheral nervous system
- 1Congenital anosmia
- 1Congenital degeneration of nervous system
- 1Congenital flaccid paralysis
- 1Congenital hypomyelinating neuropathy
- 1Congenital malformation of autonomic nervous system
- 1De Lange syndrome
- 1Donnai Barrow syndrome
- 1Dysmorphic sialidosis, congenital form
- 1Ecchordosis physaliphora
- 1Ectopic gray matter
- 1Fibrous skin tumor of tuberous sclerosis
- 1Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome
- 1Hereditary neurocutaneous angiomata
- 1HIVEP2-related intellectual disability
- 1Hypogonadism with anosmia
- 1Hypomyelination neuropathy arthrogryposis syndrome
- 1Hypomyelinogenesis congenita
- 1Male emopamil-binding protein disorder with neurological defect
- 1Neural tube defect
- 1Neuroectodermal melanolysosomal disease
- 1Neuronal choristoma
- 1Papular epidermal nevi with skyline basal cell layers syndrome
- 1Proteus syndrome
- 1Pulmonary tuberous sclerosis
- 1Sotos' syndrome
- 1Structural central nervous system abnormality
- 1Subdural hygroma with open skull wound
- 2Aganglionosis of large intestine
- 2Aganglionosis of parasympathetic nerve ganglia
- 2Amyelencephalus
- 2Angelman syndrome due to maternal monosomy 15q11q13
- 2Aprosencephaly/atelencephaly spectrum
- 2Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy
- 2CAMOS syndrome
- 2Cataract, congenital heart disease, neural tube defect syndrome
- 2Central nervous system malformation in fetus affecting obstetrical care
- 2Cerebrooculonasal syndrome
- 2Cervical myelocystocele
- 2Chaotic conus spinal cord lipoma
- 2CIMDAG syndrome
- 2Cockayne syndrome
- 2Combined immunodeficiency with faciooculoskeletal anomalies syndrome
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