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700364009: Neurodevelopmental disorder (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2989930017 Neurodevelopmental disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2990210019 Neurodevelopmental disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3787431019 Neurodevelopmental disorder is a behavioral and cognitive disorder with onset during the developmental period that involves impaired or aberrant development of intellectual, motor, or social functions. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3787432014 Neurodevelopmental disorder is a behavioural and cognitive disorder with onset during the developmental period that involves impaired or aberrant development of intellectual, motor, or social functions. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
2989930017 Neurodevelopmental disorder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2989930017 Neurodevelopmental disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2990210019 Neurodevelopmental disorder (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2990210019 Neurodevelopmental disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2990285016 Neurodevelopmental disorder is a behavioural and cognitive disorder with onset during the developmental period that involve impaired or aberrant development of intellectual, motor, or social functions. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
2990286015 Neurodevelopmental disorder is a behavioral and cognitive disorder with onset during the developmental period that involve impaired or aberrant development of intellectual, motor, or social functions. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3787431019 Neurodevelopmental disorder is a behavioral and cognitive disorder with onset during the developmental period that involves impaired or aberrant development of intellectual, motor, or social functions. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3787432014 Neurodevelopmental disorder is a behavioural and cognitive disorder with onset during the developmental period that involves impaired or aberrant development of intellectual, motor, or social functions. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5441081000241116 trouble neurodéveloppemental fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5441081000241116 trouble neurodéveloppemental fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

742 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neurodevelopmental disorder Is a Developmental disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Neurodevelopmental disorder Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Retardation of physical development (disorder) Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Developmental mental disorder Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Developmental disorder of motor function Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
myasthénie congénitale et du développement Is a False Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Developmental dyslexia Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
History of neurodevelopmental disorder Associated finding True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept) 2
On examination - neurodevelopmental disorder Is a False Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Secondary neurodevelopmental disorder (disorder) Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
5q31.3 microdeletion syndrome Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Neurodevelopmental disorder of fetus Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Prader-Willi syndrome Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
No neurodevelopmental disorder present (situation) Associated finding True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept) 1
Neurodevelopmental disorder due to maternal use of alcohol (disorder) Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic neurological disorder characterized by infantile onset of progressive leukoencephalopathy, microcephaly, severe global developmental delay, and spasticity resulting in quadriparesis and posture deformation. Additional features include an abnormally exaggerated startle reflex, seizures, dystonia, and hypomimia or amimia, as well as progressive chest deformities and contractures of large and hyperextensibility of small joints, among others. Thin corpus callosum is a prominent feature in brain imaging, in addition to white matter abnormalities consistent with leukoencephalopathy. Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Intelligenzminderung Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic disease characterized by childhood onset of multiple endocrine manifestations in combination with central and peripheral nervous system abnormalities. Reported signs and symptoms include postnatal growth retardation, moderate intellectual disability, hypogonadotropic hypogonadism, insulin-dependent diabetes mellitus, central hypothyroidism, demyelinating sensorimotor polyneuropathy, and cerebellar and pyramidal signs. Progressive hearing loss and a hypoplastic pituitary gland have also been described. Brain imaging shows moderate white matter abnormalities. Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Developmental and epileptic encephalopathy (disorder) Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
A type of epilepsy characterized by frequent epileptiform activity associated with developmental slowing and often regression on the background of previously normal development. In this type of epilepsy the frequent seizures and/or epileptiform discharges, rather than underlying etiology is thought to be the only cause of developmental impairment. Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Interferon regulatory factor 2 binding protein like-related regressive neurodevelopmental disorder, dystonia, seizures syndrome (disorder) Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome (disorder) Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
CHD8 overgrowth syndrome Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Jansen-de Vries syndrome (disorder) Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Alkuraya Kucinskas syndrome Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)
Oculogastrointestinal neurodevelopmental syndrome Is a True Neurodevelopmental disorder Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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