Mowat-Wilson syndrome 703535000
SNOMED CT code
SNOMED code | 703535000 |
---|---|
name | Mowat-Wilson syndrome |
status | active |
date introduced | 2014-07-31 |
fully specified name(s) | Mowat-Wilson syndrome (disorder) |
synonyms |
|
attributes - group1 | |
Finding site | Large intestine part 119214008 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Dilatation 25322007 |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Finding site | Large intestine part 119214008 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Hypertrophy 56246009 |
Occurrence | Congenital 255399007 |
attributes - group3 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Finding site | Autonomic nerve structure 53520000 |
Occurrence | Congenital 255399007 |
attributes - group4 | |
Finding site | Structure of peripheral part of autonomic nervous system 429921001 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
attributes - group5 | |
Interprets | Intellectual ability 247573007 |
Has interpretation | Impaired 260379002 |
attributes - group6 | |
Interprets | Adaptation behavior 406208005 |
Has interpretation | Impaired 260379002 |
parents | |
children | Mowat-Wilson syndrome due to monosomy 2q22 890118006 |
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 Mowat-Wilson syndrome 703535000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Mowat-Wilson syndrome 703535000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Disorder of the peripheral nervous system 42658009 Congenital anomaly of the peripheral nervous system 22133005 Hirschsprung's disease 204739008 Mowat-Wilson syndrome 703535000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Mowat-Wilson syndrome 703535000 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Mowat-Wilson syndrome 703535000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Disorder of autonomic nervous system 15241006 Inherited autonomic nervous system disorder 722997000 Mowat-Wilson syndrome 703535000 |
ancestors | sorted most to least specific
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cpt crosswalks |
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