Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome 722108000
SNOMED CT code
SNOMED code | 722108000 |
---|---|
name | Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (disorder) |
synonyms | Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Retinal structure 5665001 |
Associated morphology | Dystrophy 4720007 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Bone structure 272673000 |
Associated morphology | Dysplasia 25723000 |
attributes - group5 | |
Interprets | Height / growth measure 271603002 |
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 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Disorder of skeletal system 88230002 Skeletal dysplasia 105986008 Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome 722108000 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 retinitis pigmentosa 232052009 Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome 722108000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome 722108000 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome 722108000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome 722108000 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome 722108000 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Globe finding 246915008 Retina finding 399858007 Retinal disorder 29555009 Congenital anomaly of retina 49381001 Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome 722108000 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Sensorineural hearing loss 60700002 Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome 722108000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome 722108000 |
ancestors | sorted most to least specific
|
cpt crosswalks |
Thank you for choosing Find-A-Code, please Sign In to remove ads.