Encephalopathy due to mitochondrial and peroxisomal fission defect 1236807002
SNOMED CT code
| SNOMED code | 1236807002 |
|---|---|
| name | Encephalopathy due to mitochondrial and peroxisomal fission defect |
| status | active |
| date introduced | 2022-07-31 |
| fully specified name(s) | Encephalopathy due to mitochondrial and peroxisomal fission defect (disorder) |
| synonyms | Encephalopathy due to mitochondrial and peroxisomal fission defect |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Finding site | Brain structure 12738006 |
| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group4 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| attributes - group5 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 Encephalopathy due to mitochondrial and peroxisomal fission defect 1236807002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Inherited metabolic disorder of nervous system 128190004 Encephalopathy due to mitochondrial and peroxisomal fission defect 1236807002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Mitochondrial cytopathy 240096000 Encephalopathy due to mitochondrial and peroxisomal fission defect 1236807002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Encephalopathy due to mitochondrial and peroxisomal fission defect 1236807002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic encephalopathy 50122000 Encephalopathy due to mitochondrial and peroxisomal fission defect 1236807002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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