Ectodermal dysplasia syndactyly syndrome 771335004
SNOMED CT code
| SNOMED code | 771335004 |
|---|---|
| name | Ectodermal dysplasia syndactyly syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Ectodermal dysplasia syndactyly syndrome (disorder) |
| synonyms | Ectodermal dysplasia syndactyly syndrome |
| attributes - group4 | |
| Finding site | Ectoderm structure 63206006 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dysplasia 25723000 |
| Occurrence | Congenital 255399007 |
| attributes - group1 | |
| Finding site | Tooth structure 38199008 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Finding site | Digit structure 82680008 |
| Associated morphology | Congenital abnormal fusion 37764001 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Absence 418560003 |
| Finding site | Hair structure 386045008 |
| Occurrence | Congenital 255399007 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Hereditary disorder of tooth 1148766007 Ectodermal dysplasia syndactyly syndrome 771335004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 Ectodermal dysplasia with hair-tooth defects 239027006 Ectodermal dysplasia syndactyly syndrome 771335004 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Congenital anomaly of hair 65033000 Congenital alopecia 2965006 Ectodermal dysplasia syndactyly syndrome 771335004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Ectodermal dysplasia syndactyly syndrome 771335004 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Ectodermal dysplasia syndactyly syndrome 771335004 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 Syndactyly 373413006 Ectodermal dysplasia syndactyly syndrome 771335004 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 Ectodermal dysplasia syndactyly syndrome 771335004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Ectodermal dysplasia syndactyly syndrome 771335004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com