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74925009: Kernicterus (morphologic abnormality)


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
124439017 Kernicterus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
124440015 Nuclear jaundice en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
815478018 Kernicterus (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Kernicterus Is a Pigment deposition true Inferred relationship Some
Kernicterus Is a Damage true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Kernicterus due to isoimmunization Associated morphology False Kernicterus Inferred relationship Some 5
Kernicterus of newborn Associated morphology False Kernicterus Inferred relationship Some 1
Kernicterus due to isoimmunization Associated morphology False Kernicterus Inferred relationship Some 1
Kernicterus not due to isoimmunization Associated morphology False Kernicterus Inferred relationship Some 1
Kernicterus of newborn NOS Associated morphology False Kernicterus Inferred relationship Some 1
[X]Other specified kernicterus Associated morphology False Kernicterus Inferred relationship Some 1
Kernicterus of newborn NOS Associated morphology False Kernicterus Inferred relationship Some 1
Kernicterus of newborn Associated morphology True Kernicterus Inferred relationship Some 1
Kernicterus not due to isoimmunization Associated morphology False Kernicterus Inferred relationship Some 1
Kernicterus due to isoimmunization Associated morphology True Kernicterus Inferred relationship Some 1
A rare neurologic disease characterized by lethargy, hypotonia, poor feeding, opisthotonus, and a typical high-pitched cry due to bilirubin accumulation in the globus pallidus, sub-thalamic nuclei, and other brain regions, resulting from severe neonatal unconjugated hyperbilirubinemia. Onset of symptoms is typically within the first three to five days of life. Additional features include fever, apnea, seizures, and coma. Respiratory failure or refractory seizures may lead to a fatal outcome. Associated morphology True Kernicterus Inferred relationship Some 1
A rare neurologic disease characterized by the chronic consequences of bilirubin toxicity in the globus pallidus, sub-thalamic nuclei, and other brain regions, after exposure to high levels of unconjugated bilirubin in the neonatal period. Symptoms begin after the acute phase of bilirubin encephalopathy in the first year of life, evolve slowly over several years, and include mild to severe extrapyramidal disturbances (especially dystonia and athetosis), auditory neuropathy spectrum disorder, and oculomotor and dental abnormalities. Associated morphology True Kernicterus Inferred relationship Some 1

This concept is not in any reference sets

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