Retinal detachment and occipital encephalocele 703542000
SNOMED CT code
| SNOMED code | 703542000 |
|---|---|
| name | Retinal detachment and occipital encephalocele |
| status | active |
| date introduced | 2014-07-31 |
| fully specified name(s) | Retinal detachment and occipital encephalocele (disorder) |
| synonyms |
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| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Developmental failure of fusion 371520008 |
| Finding site | Bone structure of cranium 89546000 |
| attributes - group4 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Developmental failure of fusion 371520008 |
| Finding site | Structure of occipitomastoid suture of skull 57250008 |
| attributes - group1 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Macula lutea structure 82859000 |
| attributes - group5 | |
| Finding site | Vitreous body structure 47538007 |
| Associated morphology | Atrophy 13331008 |
| attributes - group6 | |
| Occurrence | Congenital 255399007 |
| Finding site | Brain structure 12738006 |
| Associated morphology | Hernia 414403008 |
| attributes - group9 | |
| Associated morphology | Atrophy 13331008 |
| Finding site | Peripheral retina 264141008 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Disorder of vitreous body 76682005 Vitreous degeneration 60189009 Vitreoretinal degeneration 247182006 Retinal detachment and occipital encephalocele 703542000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Musculoskeletal and connective tissue disorder 312225001 Retinal detachment and occipital encephalocele 703542000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Connective tissue hereditary disorder 363045008 Retinal detachment and occipital encephalocele 703542000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Retinal detachment and occipital encephalocele 703542000 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Retinal detachment and occipital encephalocele 703542000 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 Retinal detachment and occipital encephalocele 703542000 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Retinal detachment and occipital encephalocele 703542000 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Globe finding 246915008 Retina finding 399858007 Macula finding 247143009 Macular disorder 312999006 Degenerative disorder of macula 422338006 Retinal detachment and occipital encephalocele 703542000 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Joint finding 118952005 Cranial suture finding 248387005 Occipital encephalocele 42376006 Retinal detachment and occipital encephalocele 703542000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Retinal detachment and occipital encephalocele 703542000 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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