Otopalatodigital syndrome spectrum disorder 784010006
SNOMED CT code
| SNOMED code | 784010006 |
|---|---|
| name | Otopalatodigital syndrome spectrum disorder |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Otopalatodigital syndrome spectrum disorder (disorder) |
| synonyms |
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| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dysplasia 25723000 |
| Finding site | Bone structure 272673000 |
| Occurrence | Congenital 255399007 |
| parents |
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| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Disorder of skeletal system 88230002 Skeletal dysplasia 105986008 Otopalatodigital syndrome spectrum disorder 784010006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked dominant hereditary disease 1162984000 Otopalatodigital syndrome spectrum disorder 784010006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Otopalatodigital syndrome spectrum disorder 784010006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Otopalatodigital syndrome spectrum disorder 784010006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Otopalatodigital syndrome spectrum disorder 784010006 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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