Lissencephaly syndrome Norman Roberts type 717977003
SNOMED CT code
| SNOMED code | 717977003 |
|---|---|
| name | Lissencephaly syndrome Norman Roberts type |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Lissencephaly syndrome Norman Roberts type (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Bone structure of head 272679001 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Brain structure 12738006 |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Congenital anomaly of central nervous system 128124001 Disorder of neuronal migration and differentiation 253146009 Lissencephaly 204036008 Type 1 lissencephaly 253147000 Lissencephaly syndrome Norman Roberts type 717977003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Congenital anomaly of head 87290003 Congenital abnormality of skull and face bones 268239009 Lissencephaly syndrome Norman Roberts type 717977003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Lissencephaly syndrome Norman Roberts type 717977003 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Lissencephaly syndrome Norman Roberts type 717977003 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 Lissencephaly syndrome Norman Roberts type 717977003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Lissencephaly syndrome Norman Roberts type 717977003 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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