Ketoacidosis due to monocarboxylate transporter-1 deficiency 1216941002
SNOMED CT code
| SNOMED code | 1216941002 |
|---|---|
| name | Ketoacidosis due to monocarboxylate transporter-1 deficiency |
| status | active |
| date introduced | 2022-04-30 |
| fully specified name(s) | Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder) |
| synonyms | Ketoacidosis due to monocarboxylate transporter-1 deficiency |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic disorder of transport 111394006 Ketoacidosis due to monocarboxylate transporter-1 deficiency 1216941002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Ketoacidosis due to monocarboxylate transporter-1 deficiency 1216941002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of acid-base balance 26436007 Acidosis 51387008 Metabolic acidosis 59455009 Metabolic acidosis, increased anion gap (IAG) 25998009 Metabolic acidosis, IAG, accumulation of organic acids 51294009 Ketoacidosis 56051008 Ketoacidosis due to monocarboxylate transporter-1 deficiency 1216941002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Ketoacidosis due to monocarboxylate transporter-1 deficiency 1216941002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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