Lissencephaly type 1 due to doublecortin gene mutation 715780008
SNOMED CT code
| SNOMED code | 715780008 |
|---|---|
| name | Lissencephaly type 1 due to doublecortin gene mutation |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Lissencephaly type 1 due to doublecortin gene mutation (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Brain structure 12738006 |
| 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 Lissencephaly type 1 due to doublecortin gene mutation 715780008 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 Disorder of neuronal migration and differentiation 253146009 Lissencephaly 204036008 Type 1 lissencephaly 253147000 Lissencephaly type 1 due to doublecortin gene mutation 715780008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Lissencephaly type 1 due to doublecortin gene mutation 715780008 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 type 1 due to doublecortin gene mutation 715780008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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