Microphthalmia with linear skin defect syndrome 721879006
SNOMED CT code
| SNOMED code | 721879006 |
|---|---|
| name | Microphthalmia with linear skin defect syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Microphthalmia with linear skin defect syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Skin structure 39937001 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Entire eye proper 1290040004 |
| Associated morphology | Congenital smallness 41086002 |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked dominant hereditary disease 1162984000 Microphthalmia with linear skin defect syndrome 721879006 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 Microphthalmia with linear skin defect syndrome 721879006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Microphthalmia with linear skin defect syndrome 721879006 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Microphthalmia with linear skin defect syndrome 721879006 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Microphthalmia with linear skin defect syndrome 721879006 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 Microphthalmia with linear skin defect syndrome 721879006 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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