Rambaud Gallian syndrome 724002003
SNOMED CT code
| SNOMED code | 724002003 |
|---|---|
| name | Rambaud Gallian syndrome |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Finding site | Retinal structure 5665001 |
| attributes - group4 | |
| Associated morphology | Hyaline degeneration 19010006 |
| Finding site | Structure of small blood vessel (organ) 27915009 |
| attributes - group5 | |
| Associated morphology | Pathologic calcification 18115005 |
| Finding site | Cerebrum 83678007 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Hereditary degenerative disease of central nervous system 106018006 Rambaud Gallian syndrome 724002003 SNOMED CT Concept 138875005 Clinical finding 404684003 Neurological lesion 299735001 Lesion of brain 301766008 Cerebral calcification 17944005 Rambaud Gallian syndrome 724002003 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Globe finding 246915008 Retina finding 399858007 Retinal disorder 29555009 Retinal ischemia 26468004 Rambaud Gallian syndrome 724002003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Vascular degeneration 280871000 Rambaud Gallian syndrome 724002003 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Rambaud Gallian syndrome 724002003 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Rambaud Gallian syndrome 724002003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Rambaud Gallian syndrome 724002003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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