15q overgrowth syndrome 771477003
SNOMED CT code
SNOMED code | 771477003 |
---|---|
name | 15q overgrowth syndrome |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | 15q overgrowth syndrome (disorder) |
synonyms | 15q overgrowth syndrome |
attributes - group2 | |
Associated morphology | Partial trisomy 133849008 |
Finding site | Long arm of chromosome 312242007 |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
attributes - group4 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Partial trisomy 133849008 |
Finding site | Chromosome pair 15 71678009 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Face structure 89545001 |
attributes - group3 | |
Occurrence | Congenital 255399007 |
Finding site | Kidney structure 64033007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
attributes - group5 | |
Interprets | Intellectual ability 247573007 |
Has interpretation | Impaired 260379002 |
attributes - group6 | |
Interprets | Adaptation behavior 406208005 |
Has interpretation | Impaired 260379002 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 15q overgrowth syndrome 771477003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Trisomy and partial trisomy of autosome 270521004 Partial trisomy of chromosome 15 726354002 Partial duplication of long arm of chromosome 15 1162463004 15q overgrowth syndrome 771477003 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Congenital anomaly of the kidney 44513007 15q overgrowth syndrome 771477003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Multiple malformation syndrome with early overgrowth 48637007 15q overgrowth syndrome 771477003 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 15q overgrowth syndrome 771477003 |
ancestors | sorted most to least specific
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cpt crosswalks |
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