Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome 1260129000
SNOMED CT code
| SNOMED code | 1260129000 |
|---|---|
| name | Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome |
| status | active |
| date introduced | 2022-12-31 |
| fully specified name(s) | Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome (disorder) |
| synonyms |
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| attributes - group5 | |
| Clinical course | Progressive 255314001 |
| attributes - group3 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group4 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| attributes - group7 | |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group1 | |
| Occurrence | Infancy 3658006 |
| Finding site | Optic nerve structure 18234004 |
| Associated morphology | Primary atrophy 68616007 |
| attributes - group2 | |
| Occurrence | Infancy 3658006 |
| Finding site | Peripheral nervous system structure 3058005 |
| attributes - group6 | |
| Occurrence | Infancy 3658006 |
| Finding site | Axon structure 60436000 |
| 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 Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome 1260129000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic nervous system disorder 128283000 Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome 1260129000 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Inherited optic neuropathy 312942003 Hereditary optic atrophy 26360005 Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome 1260129000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome 1260129000 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 Hereditary peripheral neuropathy 65017003 Hereditary motor and sensory neuropathy 398100001 Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome 1260129000 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Axonal neuropathy 60703000 Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome 1260129000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome 1260129000 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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