Combined oxidative phosphorylation defect type 25 1173035001
SNOMED CT code
| SNOMED code | 1173035001 |
|---|---|
| name | Combined oxidative phosphorylation defect type 25 |
| status | active |
| date introduced | 2021-09-30 |
| fully specified name(s) | Combined oxidative phosphorylation defect type 25 (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Finding site | Nervous system structure 25087005 |
| attributes - group4 | |
| Finding site | Auditory structure 91159003 |
| attributes - group1 | |
| Interprets | Hearing 47078008 |
| Has interpretation | Impaired 260379002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Inherited metabolic disorder of nervous system 128190004 Combined oxidative phosphorylation defect type 25 1173035001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Deficiency in enzyme complexes of mitochondrial respiratory chain 237987001 Combined oxidative phosphorylation defect type 25 1173035001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Mitochondrial cytopathy 240096000 Combined oxidative phosphorylation defect type 25 1173035001 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Combined oxidative phosphorylation defect type 25 1173035001 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Sensorineural hearing loss 60700002 Combined oxidative phosphorylation defect type 25 1173035001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Combined oxidative phosphorylation defect type 25 1173035001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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