VACTERL syndrome with hydrocephalus 719043002
SNOMED CT code
SNOMED code | 719043002 |
---|---|
name | VACTERL syndrome with hydrocephalus |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-esophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus (disorder) |
synonyms |
|
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Dilatation 25322007 |
Occurrence | Congenital 255399007 |
Finding site | Brain cerebrospinal fluid pathway 280371009 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 VACTERL syndrome with hydrocephalus 719043002 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 VACTERL syndrome with hydrocephalus 719043002 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Disorder of brain 81308009 Hydrocephalus 230745008 Congenital hydrocephalus 47032000 VACTERL syndrome with hydrocephalus 719043002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 VACTERL syndrome with hydrocephalus 719043002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 VACTERL syndrome with hydrocephalus 719043002 |
ancestors | sorted most to least specific
|
cpt crosswalks |
Thank you for choosing Find-A-Code, please Sign In to remove ads.