Mandibular hypoplasia, deafness, progeroid syndrome 773406003
SNOMED CT code
| SNOMED code | 773406003 |
|---|---|
| name | Mandibular hypoplasia, deafness, progeroid syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Mandibular hypoplasia, deafness, progeroid syndrome (disorder) |
| synonyms |
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| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Skin structure 39937001 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Hypoplasia 55199003 |
| Finding site | Bone structure of mandible 91609006 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Finding site | Auditory structure 91159003 |
| attributes - group4 | |
| Interprets | Hearing 47078008 |
| parents |
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| 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 Mandibular hypoplasia, deafness, progeroid syndrome 773406003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of jaw 37156001 Congenital anomaly of jaw 95473006 Congenital anomaly of mandible 128224008 Congenital micrognathism 32958008 Mandibular hypoplasia, deafness, progeroid syndrome 773406003 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Mandibular hypoplasia, deafness, progeroid syndrome 773406003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Mandibular hypoplasia, deafness, progeroid syndrome 773406003 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Mandibular hypoplasia, deafness, progeroid syndrome 773406003 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Premature aging syndrome 399959003 Mandibular hypoplasia, deafness, progeroid syndrome 773406003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic bone disease 50279003 Mandibular hypoplasia, deafness, progeroid syndrome 773406003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Mandibular hypoplasia, deafness, progeroid syndrome 773406003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital sensorineural hearing loss 700453005 Mandibular hypoplasia, deafness, progeroid syndrome 773406003 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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