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703535000: Mowat-Wilson syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1720751000168115 Microcephaly, intellectual disability and distinct features, with or without Hirschsprung disease en Synonym Active Initial character case insensitive SNOMED Clinical Terms Australian extension
3008947016 Mowat-Wilson syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3009119013 Mowat-Wilson syndrome en Synonym Active Case sensitive SNOMED CT core
3009165011 Hirschsprung disease-mental retardation syndrome en Synonym Active Case sensitive SNOMED CT core
3643142016 Hirschsprung disease-intellectual disability syndrome en Synonym Active Case sensitive SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mowat-Wilson syndrome Finding site Large intestine part true Inferred relationship Some 1
Mowat-Wilson syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Mowat-Wilson syndrome Finding site Large intestine part true Inferred relationship Some 2
Mowat-Wilson syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Mowat-Wilson syndrome Associated morphology Hypertrophy true Inferred relationship Some 2
Mowat-Wilson syndrome Associated morphology Dilatation true Inferred relationship Some 1
Mowat-Wilson syndrome Pathological process Pathological developmental process true Inferred relationship Some 3
Mowat-Wilson syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 3
Mowat-Wilson syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Mowat-Wilson syndrome Finding site Structure of peripheral part of autonomic nervous system true Inferred relationship Some 4
Mowat-Wilson syndrome Pathological process Pathological developmental process true Inferred relationship Some 4
Mowat-Wilson syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 4
Mowat-Wilson syndrome Interprets Intellectual ability true Inferred relationship Some 5
Mowat-Wilson syndrome Has interpretation Impaired true Inferred relationship Some 5
Mowat-Wilson syndrome Interprets Adaptation behaviour true Inferred relationship Some 6
Mowat-Wilson syndrome Has interpretation Impaired true Inferred relationship Some 6
Mowat-Wilson syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Mowat-Wilson syndrome Is a Digestive system hereditary disorder true Inferred relationship Some
Mowat-Wilson syndrome Is a Hirschsprung's disease true Inferred relationship Some
Mowat-Wilson syndrome Is a Hereditary disorder of nervous system false Inferred relationship Some
Mowat-Wilson syndrome Is a Intellectual disability false Inferred relationship Some
Mowat-Wilson syndrome Finding site Parasympathetic nervous system structure false Inferred relationship Some
Mowat-Wilson syndrome Finding site Autonomic nerve structure true Inferred relationship Some 3
Mowat-Wilson syndrome Associated morphology Congenital dilatation false Inferred relationship Some 4
Mowat-Wilson syndrome Associated morphology Congenital hypertrophy false Inferred relationship Some 4
Mowat-Wilson syndrome Finding site Colon structure false Inferred relationship Some 4
Mowat-Wilson syndrome Occurrence Congenital false Inferred relationship Some 5
Mowat-Wilson syndrome Associated morphology Developmental abnormality false Inferred relationship Some 5
Mowat-Wilson syndrome Finding site Structure of large intestine false Inferred relationship Some 5
Mowat-Wilson syndrome Occurrence Congenital true Inferred relationship Some 1
Mowat-Wilson syndrome Associated morphology Congenital dilatation false Inferred relationship Some 1
Mowat-Wilson syndrome Finding site Colon structure false Inferred relationship Some 1
Mowat-Wilson syndrome Occurrence Congenital true Inferred relationship Some 2
Mowat-Wilson syndrome Associated morphology Congenital hypertrophy false Inferred relationship Some 2
Mowat-Wilson syndrome Finding site Colon structure false Inferred relationship Some 2
Mowat-Wilson syndrome Is a Inherited autonomic nervous system disorder true Inferred relationship Some
Mowat-Wilson syndrome Occurrence Congenital true Inferred relationship Some 3
Mowat-Wilson syndrome Finding site Large intestine part false Inferred relationship Some 3
Mowat-Wilson syndrome Occurrence Congenital true Inferred relationship Some 4
Mowat-Wilson syndrome Finding site Large intestine part false Inferred relationship Some 4
Mowat-Wilson syndrome Associated morphology Congenital hypertrophy false Inferred relationship Some 3
Mowat-Wilson syndrome Is a Intellectual disability true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Mowat-Wilson syndrome due to monosomy 2q22 Is a True Mowat-Wilson syndrome Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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