Symphalangism Cushing type 1162837001
SNOMED CT code
SNOMED code | 1162837001 |
---|---|
name | Symphalangism Cushing type |
status | active |
date introduced | 2021-09-30 |
fully specified name(s) | Proximal interphalangeal joint symphalangism Cushing type (disorder) |
synonyms |
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attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Structure of proximal interphalangeal joint of digit 871489002 |
Associated morphology | Ankylosis 36504009 |
Pathological process | Pathological developmental process 308490002 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Symphalangism Cushing type 1162837001 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Disorder of digit 128597007 Congenital anomaly of digit 403855001 Symphalangism 253975004 Proximal interphalangeal joint symphalangism 205280007 Symphalangism Cushing type 1162837001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Symphalangism Cushing type 1162837001 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Symphalangism Cushing type 1162837001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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