Barber-Say syndrome 408537003
SNOMED CT code
| SNOMED code | 408537003 | ||
|---|---|---|---|
| name | Barber-Say syndrome | ||
| status | active | ||
| date introduced | 2004-01-31 | ||
| fully specified name(s) | Barber-Say syndrome (disorder) | ||
| synonyms | Barber-Say syndrome | ||
| attributes - group2 | |||
| Associated morphology | Dysplasia 25723000 | ||
| Pathological process | Pathological developmental process 308490002 | ||
| Occurrence | Congenital 255399007 | ||
| Finding site | Ectoderm structure 63206006 | ||
| attributes - group3 | |||
| Occurrence | Congenital 255399007 | ||
| Finding site | Mouth region structure 123851003 | ||
| Associated morphology | Congenital smallness 41086002 | ||
| Pathological process | Pathological developmental process 308490002 | ||
| attributes - group4 | |||
| Associated morphology | Morphologically abnormal structure 49755003 | ||
| Finding site | Face structure 89545001 | ||
| Occurrence | Congenital 255399007 | ||
| Pathological process | Pathological developmental process 308490002 | ||
| attributes - group5 | |||
| Associated morphology | Growth alteration 57697001 | ||
| Occurrence | Congenital 255399007 | ||
| Finding site | Hair structure 386045008 | ||
| Pathological process | Pathological developmental process 308490002 | ||
| attributes - group1 | |||
| Finding site | Skin structure 39937001 | ||
| Associated morphology | Atrophy 13331008 | ||
| parents | |||
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of head 118934005 Disease of mouth 118938008 Congenital anomaly of mouth 128334002 Microstomia 14582003 Barber-Say syndrome 408537003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative skin disorder 396325007 Atrophic condition of skin 400190005 Barber-Say syndrome 408537003 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Congenital anomaly of hair 65033000 Congenital hypertrichosis 56797000 Barber-Say syndrome 408537003 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Barber-Say syndrome 408537003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Barber-Say syndrome 408537003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 Barber-Say syndrome 408537003 | ||
| ancestors | sorted most to least specific
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| cpt crosswalks |
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