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719845008: Van den Ende-Gupta syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3318141014 Van den Ende-Gupta syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3318142019 Van den Ende-Gupta syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3318143012 Marden Walker like syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Van den Ende-Gupta syndrome Is a Inherited arthrogryposis true Inferred relationship Existential restriction modifier
Van den Ende-Gupta syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Van den Ende-Gupta syndrome Is a Amyoplasia congenita disruptive sequence true Inferred relationship Existential restriction modifier
Van den Ende-Gupta syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Van den Ende-Gupta syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Van den Ende-Gupta syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Van den Ende-Gupta syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 3
Van den Ende-Gupta syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Van den Ende-Gupta syndrome Finding site Joint structure false Inferred relationship Existential restriction modifier 4
Van den Ende-Gupta syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Van den Ende-Gupta syndrome Finding site Joint structure false Inferred relationship Existential restriction modifier 5
Van den Ende-Gupta syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 4
Van den Ende-Gupta syndrome Associated morphology Contracture false Inferred relationship Existential restriction modifier 5
Van den Ende-Gupta syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Van den Ende-Gupta syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Van den Ende-Gupta syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Van den Ende-Gupta syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Van den Ende-Gupta syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 1
Van den Ende-Gupta syndrome Finding site Joint structure false Inferred relationship Existential restriction modifier 2
Van den Ende-Gupta syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Van den Ende-Gupta syndrome Associated morphology Contracture true Inferred relationship Existential restriction modifier 2
Van den Ende-Gupta syndrome Interprets Range of joint movement true Inferred relationship Existential restriction modifier 3
Van den Ende-Gupta syndrome Has interpretation Decreased true Inferred relationship Existential restriction modifier 3
Van den Ende-Gupta syndrome Finding site Structure of joint region true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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