Francois syndrome 254150007
SNOMED CT code
SNOMED code | 254150007 |
---|---|
name | Francois syndrome |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Francois syndrome (disorder) |
synonyms |
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attributes - group3 | |
Finding site | Bone structure 272673000 |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Dystrophy 4720007 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Skin structure 39937001 |
Associated morphology | Nodule 27925004 |
attributes - group2 | |
Associated morphology | Dystrophy 4720007 |
Occurrence | Congenital 255399007 |
Finding site | Corneal structure 28726007 |
Pathological process | Pathological developmental process 308490002 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disorder of eye 62585004 Corneal degeneration 111521006 Corneal dystrophy 5587004 Congenital corneal dystrophy 1003408005 Francois syndrome 254150007 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 Francois syndrome 254150007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Francois syndrome 254150007 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Francois syndrome 254150007 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Francois syndrome 254150007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital osteodystrophy 5731000119108 Francois syndrome 254150007 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Hereditary corneal dystrophy 77797009 Francois syndrome 254150007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Francois syndrome 254150007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Francois syndrome 254150007 SNOMED CT Concept 138875005 Clinical finding 404684003 Mass of body structure 300848003 Nodule in skin or mucosa 271758006 Skin nodule 95319004 Francois syndrome 254150007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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