Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency 723552005

SNOMED CT code

SNOMED code

723552005

name

Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency

status

active

date introduced

2017-07-31

fully specified name(s)

Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency (disorder)

synonyms

Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency
Transient neonatal multiple acyl-CoA dehydrogenase deficiency
Transient neonatal glutaric acidemia type 2
Transient neonatal glutaric acidaemia type 2
Transient neonatal glutaric aciduria type 2
Transient neonatal MAD (multiple acyl-coenzyme A dehydrogenase) deficiency

attributes - group3

Occurrence

Congenital 255399007

attributes - group1

Occurrence

Neonatal 255407002

attributes - group2

Clinical course

Transitory 14803004

parents

Autosomal dominant hereditary disorder 11164009
Neonatal transient metabolic disturbance 25211000119101
Acyl-CoA dehydrogenase deficiency 82319005

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal dominant hereditary disorder 11164009
Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency 723552005

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Acute disease 2704003
Acute metabolic disorder 127339009
Neonatal transient metabolic disturbance 25211000119101
Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency 723552005

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Metabolic disease 75934005
Enzymopathy 78548001
Acyl-CoA dehydrogenase deficiency 82319005
Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency 723552005

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Neonatal transient metabolic disturbance 25211000119101
Acyl-CoA dehydrogenase deficiency 82319005
Acute metabolic disorder 127339009
Fatty acid oxidation defect 1156591005
Neonatal metabolic disorder 736652002
Enzymopathy 78548001
Acute disease 2704003
Disorder of fatty acid metabolism 39929009
Neonatal disease 22925008
Autosomal recessive hereditary disorder 85995004
Autosomal hereditary disorder 1899006
Disorder of organic acid metabolism 116021002
Finding of neonate 118188004
Disorder of lipoprotein AND/OR lipid metabolism 48286001
Inborn error of metabolism 86095007
Disorder of fetus and/or newborn 414025005
Hereditary metabolic disease 1821000146108
Congenital disease 66091009
Hereditary disease 32895009
Metabolic disease 75934005
Genetic disease 782964007
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Genetic disease 782964007

Hereditary disease 32895009

Autosomal hereditary disorder 1899006

Autosomal dominant hereditary disorder 11164009

Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency 723552005

SNOMED CT code