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782946000: Gastrocutaneous syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3756891010 Gastrocutaneous syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3756892015 Gastrocutaneous syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Gastrocutaneous syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Gastrocutaneous syndrome Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Gastrocutaneous syndrome Is a Genetic disorder of skin pigmentation true Inferred relationship Existential restriction modifier
Gastrocutaneous syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Gastrocutaneous syndrome Is a Hyperpigmentation of skin true Inferred relationship Existential restriction modifier
Gastrocutaneous syndrome Associated morphology Hyperpigmentation true Inferred relationship Existential restriction modifier 1
Gastrocutaneous syndrome Is a Disorder of upper gastrointestinal tract true Inferred relationship Existential restriction modifier
Gastrocutaneous syndrome Finding site Upper gastrointestinal tract structure true Inferred relationship Existential restriction modifier 2
Gastrocutaneous syndrome Is a Hereditary disorder of the integument 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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