Megalencephaly capillary malformation 700063005
SNOMED CT code
| SNOMED code | 700063005 |
|---|---|
| name | Megalencephaly capillary malformation |
| status | active |
| date introduced | 2014-01-31 |
| fully specified name(s) | Megalencephaly capillary malformation (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Enlargement 442021009 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Cerebrum 83678007 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Structure of capillary blood vessel 20982000 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Face structure 89545001 |
| Pathological process | Pathological developmental process 308490002 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Cardiovascular finding 106063007 Blood vessel finding 21829004 Capillary finding 248723009 Disorder of capillaries 58729003 Capillary malformation 234118009 Megalencephaly capillary malformation 700063005 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Megalencephaly capillary malformation 700063005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Megalencephaly capillary malformation 700063005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Megalencephaly capillary malformation 700063005 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 Megalencephaly capillary malformation 700063005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary cancer-predisposing syndrome 699346009 Megalencephaly capillary malformation 700063005 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Congenital anomaly of central nervous system 128124001 Congenital anomaly of brain 57148006 Congenital anomaly of cerebrum 702628006 Macroencephaly 9740002 Megalencephaly capillary malformation 700063005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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