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255398004: Childhood (qualifier value)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1224895014 Childhood - period en Synonym Active Case insensitive SNOMED CT core
380597017 Childhood en Synonym Active Case insensitive SNOMED CT core
646432014 Childhood (qualifier value) en Fully specified name Active Case insensitive SNOMED CT core


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 Period of life between birth and death true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Polyarticular juvenile idiopathic arthritis Occurrence False Childhood Inferred relationship Some
Juvenile polymyositis Occurrence True Childhood Inferred relationship Some 1
Childhood hypophosphatasia Occurrence True Childhood Inferred relationship Some 1
Childhood duodenal ulcer Occurrence False Childhood Inferred relationship Some
Childhood onset conduct-dissocial disorder Occurrence True Childhood Inferred relationship Some 1
Underweight in childhood Occurrence True Childhood Inferred relationship Some 1
Nutritional wasting in childhood Occurrence True Childhood Inferred relationship Some 1
Acute malnutrition in childhood Occurrence True Childhood Inferred relationship Some 1
Nutritional stunting in childhood Occurrence True Childhood Inferred relationship Some 1
Paediatric onset Sjögren syndrome Occurrence False Childhood Inferred relationship Some 2
Acute necrotising encephalopathy of childhood Occurrence True Childhood Inferred relationship Some 1
Gender identity disorder of childhood Occurrence True Childhood Inferred relationship Some 1
Juvenile overlap myositis Occurrence True Childhood Inferred relationship Some 1
Acute encephalopathy with biphasic seizures and late reduced diffusion Occurrence True Childhood Inferred relationship Some 1
Recurrent benign focal seizures of childhood Occurrence True Childhood Inferred relationship Some 1
Gastrooesophageal reflux in child Occurrence True Childhood Inferred relationship Some 1
Acquired megacolon in child Occurrence True Childhood Inferred relationship Some 2
Acquired megacolon in child Occurrence True Childhood Inferred relationship Some 1
Acquired epileptic aphasia Occurrence True Childhood Inferred relationship Some 1
Mucinous cystadenoma of ovary in childhood Occurrence True Childhood Inferred relationship Some 1
Serous cystadenoma of ovary in childhood Occurrence True Childhood Inferred relationship Some 1
Childhood double incontinence Occurrence False Childhood Inferred relationship Some 3
Benign occipital epilepsy of childhood - early onset variant Occurrence True Childhood Inferred relationship Some 1
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A (glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A) mutation Occurrence True Childhood Inferred relationship Some 1
Benign occipital epilepsy of childhood - late onset variant Occurrence True Childhood Inferred relationship Some 1
Coxa plana Occurrence True Childhood Inferred relationship Some 1
Familial juvenile hypertrophy of the breast Occurrence True Childhood Inferred relationship Some 1
Intellectual disability, seizures, macrocephaly, obesity syndrome Occurrence True Childhood Inferred relationship Some 5
Laing early-onset distal myopathy Occurrence True Childhood Inferred relationship Some 1
Developmental delay with autism spectrum disorder and gait instability Occurrence True Childhood Inferred relationship Some 1
Kelch like family member 9 related early-onset distal myopathy Occurrence True Childhood Inferred relationship Some 1
Hyperzincaemia and hypercalprotectinaemia Occurrence True Childhood Inferred relationship Some 1
Benign nocturnal alternating hemiplegia of childhood Occurrence True Childhood Inferred relationship Some 1
Autosomal recessive lower motor neuron disease with childhood onset Occurrence True Childhood Inferred relationship Some 2
Autosomal recessive lower motor neuron disease with childhood onset Occurrence True Childhood Inferred relationship Some 1

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Reference Sets

Qualifier value foundation reference set

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