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255398004: Childhood (qualifier value)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
380597017 Childhood en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
646432014 Childhood (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1224895014 Childhood - period en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
363351000195111 infanzia it Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
262151000077110 enfance fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2391001000117 Kindesalter de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
17931001000116 Kindheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Childhood Is a Periods of life false Inferred relationship Some
Childhood Is a Any period of life commencing after birth, but before death. true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Childhood phobic anxiety disorder (disorder) Occurrence True Childhood Inferred relationship Some 1
Childhood bronchiectasis Occurrence False Childhood Inferred relationship Some
Childhood hypophosphatasia Occurrence True Childhood Inferred relationship Some 1
Childhood duodenal ulcer Occurrence False Childhood Inferred relationship Some
Childhood growth AND/OR development finding Occurrence True Childhood Inferred relationship Some 1
Childhood growth AND/OR development alteration Occurrence True Childhood Inferred relationship Some 1
Fighting at school Occurrence False Childhood Inferred relationship Some
Truancy Occurrence False Childhood Inferred relationship Some
Childhood disorder of conduct and emotion Occurrence True Childhood Inferred relationship Some 1
Childhood or adolescent identity disorder Occurrence False Childhood Inferred relationship Some
Childhood or adolescent disorder of social functioning (disorder) Occurrence False Childhood Inferred relationship Some 1
Psychogenic feeding disorder of infancy and childhood Occurrence True Childhood Inferred relationship Some 1
Distal muscular dystrophy with juvenile onset Occurrence True Childhood Inferred relationship Some 1
Systemic onset juvenile chronic arthritis Occurrence False Childhood Inferred relationship Some
Juvenile arthritis in Crohn's disease (disorder) Occurrence False Childhood Inferred relationship Some
Juvenile arthritis in ulcerative colitis Occurrence False Childhood Inferred relationship Some
Juvenile osteochondrosis of head of humerus Occurrence False Childhood Inferred relationship Some
Anxiety disorder of childhood OR adolescence Occurrence True Childhood Inferred relationship Some 1
Chronic bullous dermatosis of childhood (disorder) Occurrence False Childhood Inferred relationship Some 5
Progressive bulbar palsy of childhood Occurrence True Childhood Inferred relationship Some 1
Progressive neuronal degeneration of childhood Occurrence True Childhood Inferred relationship Some 1
Progressive neuronal degeneration without liver cirrhosis Occurrence True Childhood Inferred relationship Some 2
épilepsie bénigne frontale de l'enfance Occurrence False Childhood Inferred relationship Some 1
épilepsie psychomotrice bénigne de l'enfance Occurrence False Childhood Inferred relationship Some 1
Benign atypical partial epilepsy in childhood Occurrence True Childhood Inferred relationship Some 1
Epilepsy with recurrent unilateral seizures in children Occurrence False Childhood Inferred relationship Some
épilepsie de l'enfance avec paroxysmes occipitaux Occurrence False Childhood Inferred relationship Some 1
A rare genetic neurological disorder characterised by late infancy to early-adolescence onset of prolonged, nocturnal seizures which begin with autonomic features (e.g. vomiting, pallor, sweating) and associate tonic eye deviation, impairment of consciousness and may evolve to a hemi-clonic or generalised convulsion. Autonomic status epilepticus may be the only clinical event in some cases. Occurrence False Childhood Inferred relationship Some
A rare genetic neurological disorder with characteristics of childhood to mid-adolescence onset of frequent, brief, diurnal simple partial seizures which usually begin with visual hallucinations (e.g. phosphenes) and/or ictal blindness and may associate non visual seizures (such as deviation of the eyes, oculo clonic seizures), forced eyelid closure and blinking and sensory hallucinations. Post-ictal headache is common while impairment of consciousness is rare. Occurrence False Childhood Inferred relationship Some
épilepsie progressive partielle chronique continue de l'enfance Occurrence False Childhood Inferred relationship Some 1
épilepsie myoclonique de la petite enfance Occurrence False Childhood Inferred relationship Some 1
A type of epilepsy that presents with typical absence seizures between 9 and 13 years of age in an otherwise normal adolescent. The typical absence seizures usually occur less than daily in the untreated state and are provoked by hyperventilation in 87 percent of cases. Generalized tonic-clonic seizures are seen in greater than 90 percent of cases, most commonly beginning shortly after onset of absence seizures. Myoclonic seizures do not occur. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram shows 3 to 5.5 Hz generalized spike-wave with a normal background. Occurrence False Childhood Inferred relationship Some 1
A rare, genetic, developmental and epileptic encephalopathy characterized by infantile onset of intractable seizures that are often febrile, and associated with cognitive and motor impairment. Occurrence False Childhood Inferred relationship Some
Alternating hemiplegia of childhood Occurrence True Childhood Inferred relationship Some 1
Conduct disorder - in family context Occurrence False Childhood Inferred relationship Some 1
Conduct disorder - unsocialised Occurrence False Childhood Inferred relationship Some 1
Depressive conduct disorder Occurrence False Childhood Inferred relationship Some 1
Central retinal vein occlusion - juvenile Occurrence True Childhood Inferred relationship Some 1
Neovascularization of eye due to juvenile central retinal vein occlusion Occurrence True Childhood Inferred relationship Some 1
Macular oedema due to juvenile central retinal vein occlusion Occurrence True Childhood Inferred relationship Some 1
Transient erythroblastopenia of childhood Occurrence True Childhood Inferred relationship Some 3
Irritable bowel syndrome variant of childhood Occurrence False Childhood Inferred relationship Some
Irritable bowel syndrome variant of childhood with diarrhea Occurrence False Childhood Inferred relationship Some
Irritable bowel syndrome variant of childhood with constipation Occurrence False Childhood Inferred relationship Some
Juvenile Graves' disease Occurrence False Childhood Inferred relationship Some 3
Total hexosaminidase deficiency - juvenile Occurrence True Childhood Inferred relationship Some 2
B variant hexosaminidase A deficiency - juvenile Occurrence True Childhood Inferred relationship Some 1
Juvenile plantar dermatosis Occurrence False Childhood Inferred relationship Some
Classical juvenile pityriasis rubra pilaris Occurrence False Childhood Inferred relationship Some 4
Circumscribed juvenile pityriasis rubra pilaris Occurrence False Childhood Inferred relationship Some 4
Atypical juvenile pityriasis rubra pilaris Occurrence False Childhood Inferred relationship Some 4
Juvenile aponeurotic fibroma Occurrence False Childhood Inferred relationship Some 2
Juvenile elastofibromatosis (disorder) Occurrence True Childhood Inferred relationship Some 2
Juvenile colloid milium Occurrence False Childhood Inferred relationship Some 3
Childhood granulomatous periorificial dermatitis (disorder) Occurrence True Childhood Inferred relationship Some 2
arthrite chronique juvénile Occurrence False Childhood Inferred relationship Some
Early onset pauciarticular chronic arthritis Occurrence False Childhood Inferred relationship Some
Late onset pauciarticular chronic arthritis Occurrence False Childhood Inferred relationship Some
Early onset polyarticular juvenile chronic arthritis Occurrence True Childhood Inferred relationship Some 1
Late onset polyarticular juvenile chronic arthritis Occurrence False Childhood Inferred relationship Some
Juvenile rheumatoid arthritis Occurrence False Childhood Inferred relationship Some
Juvenile psoriatic arthritis Occurrence False Childhood Inferred relationship Some
Juvenile psoriatic arthritis with psoriasis Occurrence False Childhood Inferred relationship Some
Juvenile psoriatic arthritis without psoriasis Occurrence False Childhood Inferred relationship Some
Juvenile ankylosing spondylitis Occurrence False Childhood Inferred relationship Some
Juvenile spondyloarthropathy (disorder) Occurrence False Childhood Inferred relationship Some
Juvenile reactive arthritis Occurrence False Childhood Inferred relationship Some
Juvenile reactive arthritis triad Occurrence False Childhood Inferred relationship Some
Juvenile arthritis of inflammatory bowel disease Occurrence False Childhood Inferred relationship Some
Juvenile scleroderma Occurrence False Childhood Inferred relationship Some
Adult onset Still's disease Occurrence False Childhood Inferred relationship Some
Severe autosomal recessive muscular dystrophy of childhood - North African type Occurrence False Childhood Inferred relationship Some 1
Juvenile tabes dorsalis Occurrence False Childhood Inferred relationship Some
Dysmorphic sialidosis, juvenile form Occurrence True Childhood Inferred relationship Some 1
Reactive attachment disorder of infancy OR early childhood, disinhibited type Occurrence False Childhood Inferred relationship Some 2
Parental withholding from school Occurrence False Childhood Inferred relationship Some
Papillary intralymphatic angioendothelioma of childhood (disorder) Occurrence False Childhood Inferred relationship Some
Juvenile fibroadenoma of breast Occurrence False Childhood Inferred relationship Some 3
Childhood or adolescent antisocial behavior Occurrence False Childhood Inferred relationship Some
Juvenile osteochondrosis of capitulum of humerus (disorder) Occurrence False Childhood Inferred relationship Some
Childhood emotional disorder Occurrence True Childhood Inferred relationship Some 1
Childhood disinhibited attachment disorder Occurrence True Childhood Inferred relationship Some 1
Juvenile chronic myeloid leukaemia Occurrence False Childhood Inferred relationship Some 2
Juvenile elastoma Occurrence False Childhood Inferred relationship Some 2
Primitive rage Occurrence False Childhood Inferred relationship Some
Separation anxiety disorder of childhood Occurrence True Childhood Inferred relationship Some 1
Childhood type dermatomyositis Occurrence False Childhood Inferred relationship Some 3
Overanxious disorder of childhood Occurrence True Childhood Inferred relationship Some 1
A group of epilepsies characterized by age-dependent occurrence of drug responsive focal seizures in otherwise normal children. Seizures are focal motor or sensory with or without impaired awareness and may evolve to bilateral tonic-clonic seizures. Remission usually occurs by puberty. Development and cognition are typically normal. Neurological examination is normal. No significant structural lesions of the brain are present, and presumed genetic factors have an important role. The electroencephalogram (EEG) background activity is normal. Seizure semiology and EEG features are specific for each of the syndromes included in this group. Occurrence False Childhood Inferred relationship Some 1
Juvenile epithelial corneal dystrophy (disorder) Occurrence False Childhood Inferred relationship Some
Conduct disorder, childhood-onset type Occurrence True Childhood Inferred relationship Some 1
Juvenile GM1 gangliosidosis Occurrence True Childhood Inferred relationship Some 2
Oppositional defiant disorder Occurrence True Childhood Inferred relationship Some 1
Chronic polyarticular juvenile rheumatoid arthritis Occurrence False Childhood Inferred relationship Some
Progressive sclerosing poliodystrophy Occurrence False Childhood Inferred relationship Some 3
Reactive attachment disorder of infancy OR early childhood, inhibited type Occurrence False Childhood Inferred relationship Some 2
Runaway reaction of childhood Occurrence False Childhood Inferred relationship Some
Cerebral degeneration in childhood Occurrence True Childhood Inferred relationship Some 2
Sibling rivalry Occurrence False Childhood Inferred relationship Some
Hemolytic uremic syndrome of childhood Occurrence True Childhood Inferred relationship Some 10
Anxiety disorder of adolescence Occurrence True Childhood Inferred relationship Some 2

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This concept is not in any reference sets

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