Childhood encephalopathy due to thiamine pyrophosphokinase deficiency 773668008
SNOMED CT code
| SNOMED code | 773668008 |
|---|---|
| name | Childhood encephalopathy due to thiamine pyrophosphokinase deficiency |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Childhood encephalopathy due to thiamine pyrophosphokinase deficiency (disorder) |
| synonyms |
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| attributes - group1 | |
| Occurrence | Childhood 255398004 |
| Finding site | Brain structure 12738006 |
| attributes - group2 | |
| Due to | Deficiency of thiamine pyrophosphokinase 124344007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Childhood encephalopathy due to thiamine pyrophosphokinase deficiency 773668008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic encephalopathy 50122000 Childhood encephalopathy due to thiamine pyrophosphokinase deficiency 773668008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Childhood encephalopathy due to thiamine pyrophosphokinase deficiency 773668008 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Central nervous system complication 87536007 Childhood encephalopathy due to thiamine pyrophosphokinase deficiency 773668008 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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