Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008
SNOMED CT code
SNOMED code | 763688008 |
---|---|
name | Deafness, encephaloneuropathy, obesity, valvulopathy syndrome |
status | active |
date introduced | 2018-07-31 |
fully specified name(s) | Deafness, encephaloneuropathy, obesity, valvulopathy syndrome (disorder) |
synonyms |
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attributes - group6 | |
Interprets | Hearing 47078008 |
attributes - group5 | |
Due to | Coenzyme Q10 deficiency 724575009 |
attributes - group3 | |
Occurrence | Congenital 255399007 |
Finding site | Ear structure 117590005 |
attributes - group4 | |
Occurrence | Congenital 255399007 |
Finding site | Peripheral nerve structure 84782009 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Finding site | Skeletal muscle structure 127954009 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Brain structure 12738006 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Hearing loss associated with syndrome 232333009 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Myoneural disorder 257277002 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of ear 25906001 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Disorder of brain 81308009 Mitochondrial encephalomyopathy 447292006 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Secondary myopathy 60738003 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008 SNOMED CT Concept 138875005 Clinical finding 404684003 General finding of soft tissue 248402002 Disorder of soft tissue 19660004 Peripheral nerve disease 302226006 Peripheral neuropathy due to metabolic disorder 710360007 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Central nervous system complication 87536007 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Deafness, encephaloneuropathy, obesity, valvulopathy syndrome 763688008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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