FOXG1 syndrome 702450004
SNOMED CT code
SNOMED code | 702450004 |
---|---|
name | FOXG1 syndrome |
status | active |
date introduced | 2014-07-31 |
fully specified name(s) | FOXG1 syndrome (disorder) |
synonyms | FOXG1 syndrome |
attributes - group1 | |
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 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 FOXG1 syndrome 702450004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Mental disorder 74732009 Developmental mental disorder 129104009 Disorder of psychological development 192562009 Pervasive developmental disorder 35919005 FOXG1 syndrome 702450004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 FOXG1 syndrome 702450004 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 FOXG1 syndrome 702450004 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 FOXG1 syndrome 702450004 |
ancestors | sorted most to least specific
|
cpt crosswalks |
Thank you for choosing Find-A-Code, please Sign In to remove ads.