Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome 1187115008
SNOMED CT code
| SNOMED code | 1187115008 |
|---|---|
| name | Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome |
| status | active |
| date introduced | 2021-11-30 |
| fully specified name(s) | Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome (disorder) |
| synonyms | Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure of extremity 48566001 |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Finding site | Digit structure 82680008 |
| Associated morphology | Supernumerary structure 91431006 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group2 | |
| Finding site | Hair structure 386045008 |
| Associated morphology | Growth alteration 57697001 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Dysostosis 109420003 Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome 1187115008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome 1187115008 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Skin finding 106076001 Hair finding 247522004 Disorder of hair 279425004 Disorder of hair growth 267808001 Hypertrichosis 29966009 Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome 1187115008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome 1187115008 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome 1187115008 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome 1187115008 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 Polydactyly 367506006 Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome 1187115008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Multiple malformation syndrome with limb defect as major feature 41443008 Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome 1187115008 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Congenital anomaly of limb 60475009 Congenital dysplasia of limb 88631000119105 Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome 1187115008 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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