Ectodermal dysplasia and sensorineural deafness syndrome 732953008
SNOMED CT code
SNOMED code | 732953008 |
---|---|
name | Ectodermal dysplasia and sensorineural deafness syndrome |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Ectodermal dysplasia and sensorineural deafness syndrome (disorder) |
synonyms | Ectodermal dysplasia and sensorineural deafness syndrome |
attributes - group2 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
Finding site | Skin structure 39937001 |
Pathological process | Pathological developmental process 308490002 |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Finding site | Ectoderm structure 63206006 |
Occurrence | Congenital 255399007 |
Associated morphology | Dysplasia 25723000 |
attributes - group3 | |
Finding site | Auditory structure 91159003 |
attributes - group4 | |
Interprets | Hearing 47078008 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Hearing loss associated with syndrome 232333009 Ectodermal dysplasia and sensorineural deafness syndrome 732953008 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Ectodermal dysplasia and sensorineural deafness syndrome 732953008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Ectodermal dysplasia and sensorineural deafness syndrome 732953008 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Ectodermal dysplasia and sensorineural deafness syndrome 732953008 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Sensorineural hearing loss 60700002 Ectodermal dysplasia and sensorineural deafness syndrome 732953008 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 and sensorineural deafness syndrome 732953008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 Ectodermal dysplasia and sensorineural deafness syndrome 732953008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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