Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome 773628009
SNOMED CT code
SNOMED code | 773628009 |
---|---|
name | Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome (disorder) |
synonyms |
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attributes - group2 | |
Finding site | Face structure 89545001 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Morphologically abnormal structure 49755003 |
attributes - group3 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Congenital smallness 41086002 |
Finding site | Entire eye proper 1290040004 |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Finding site | Palatal structure 72914001 |
Occurrence | Congenital 255399007 |
Associated morphology | Developmental failure of fusion 371520008 |
attributes - group4 | |
Finding site | Bone structure of cranium 89546000 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Dysplasia 25723000 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome 773628009 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome 773628009 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome 773628009 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Congenital anomaly of visual system 127329003 Congenital anomaly of eye 19416009 Microphthalmos 61142002 Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome 773628009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome 773628009 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 Frontonasal dysplasia sequence 86610004 Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome 773628009 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Orofacial cleft 449790007 Cleft palate 87979003 Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome 773628009 |
ancestors | sorted most to least specific
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cpt crosswalks |
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