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703535000: Mowat-Wilson syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3008947016 Mowat-Wilson syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3009119013 Mowat-Wilson syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3009165011 Hirschsprung disease-mental retardation syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643142016 Hirschsprung disease-intellectual disability syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


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

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

This concept is not in any reference sets

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