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720569006: Brachydactyly type A2 (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
3321274011 Brachydactyly type A2 (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3321275012 Brachydactyly type A2 en Synonym Active Only initial character case insensitive SNOMED CT core module
3321276013 Brachydactyly Mohr Wriedt type en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Brachydactyly type A2 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Brachydactyly type A2 Is a Brachydactyly true Inferred relationship Existential restriction modifier
Brachydactyly type A2 Associated morphology Abnormally short growth true Inferred relationship Existential restriction modifier 1
Brachydactyly type A2 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Brachydactyly type A2 Finding site Entire digit true Inferred relationship Existential restriction modifier 1
Brachydactyly type A2 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Brachydactyly type A2 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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