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721902002: Schilbach Rott 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
3326803010 Schilbach Rott syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3326804016 Schilbach Rott syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3326805015 Hypotelorism, cleft palate, hypospadias syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Schilbach Rott syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Schilbach Rott syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Schilbach Rott syndrome Is a Syndactyly true Inferred relationship Existential restriction modifier
Schilbach Rott syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Schilbach Rott syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Schilbach Rott syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 2
Schilbach Rott syndrome Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier 3
Schilbach Rott syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Schilbach Rott syndrome Finding site Digit structure false Inferred relationship Existential restriction modifier 3
Schilbach Rott syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Schilbach Rott syndrome Finding site Digit structure true Inferred relationship Existential restriction modifier 1
Schilbach Rott syndrome Associated morphology Congenital abnormal fusion true Inferred relationship Existential restriction modifier 1
Schilbach Rott syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Schilbach Rott syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Schilbach Rott syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Schilbach Rott syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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