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715721005: Brachydactyly type A4 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3303511011 Brachydactyly type A4 (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3303512016 Brachydactyly type A4 en Synonym Active Only initial character case insensitive SNOMED CT core module
3303513014 Brachydactyly Temtamy 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 A4 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Brachydactyly type A4 Is a Brachymesophalangia true Inferred relationship Existential restriction modifier
Brachydactyly type A4 Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Brachydactyly type A4 Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Brachydactyly type A4 Associated morphology Abnormally short growth true Inferred relationship Existential restriction modifier 1
Brachydactyly type A4 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Brachydactyly type A4 Finding site Entire phalanx false Inferred relationship Existential restriction modifier 1
Brachydactyly type A4 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Brachydactyly type A4 Finding site Entire middle phalanx true Inferred relationship Existential restriction modifier 1
Brachydactyly type A4 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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