Genochondromatosis type 2 725904009
SNOMED CT code
| SNOMED code | 725904009 |
|---|---|
| name | Genochondromatosis type 2 |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Genochondromatosis type 2 (disorder) |
| synonyms | Genochondromatosis type 2 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure 272673000 |
| Associated morphology | Dysplasia 25723000 |
| attributes - group2 | |
| Finding site | Cartilage structure 771314001 |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| 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 Genochondromatosis type 2 725904009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Connective tissue hereditary disorder 363045008 Genochondromatosis type 2 725904009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Genochondromatosis type 2 725904009 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Genochondromatosis type 2 725904009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Congenital connective tissue disorder 363039000 Congenital anomaly of cartilage 67988000 Disorganized development of cartilaginous and fibrous components of the skeleton 254140006 Genochondromatosis 389264005 Genochondromatosis type 2 725904009 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Cartilage finding 118954006 Cartilage disorder 50927007 Osteochondropathy 77881008 Genochondromatosis type 2 725904009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Genochondromatosis type 2 725904009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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