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205317004: Brachymesophalangia (disorder)


Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
314843010 Brachymesophalangia en Synonym Active Case insensitive SNOMED CT core
590665017 Brachymesophalangia (disorder) en Fully specified name Active Case insensitive SNOMED CT core


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Brachymesophalangia Pathological process Pathological developmental process true Inferred relationship Some 1
Brachymesophalangia Finding site Entire middle phalanx true Inferred relationship Some 1
Brachymesophalangia Finding site Limb structure false Inferred relationship Some 2
Brachymesophalangia Associated morphology Congenital anomaly false Inferred relationship Some 2
Brachymesophalangia Is a Brachyphalangia true Inferred relationship Some
Brachymesophalangia Finding site Phalanx structure false Inferred relationship Some 1
Brachymesophalangia Associated morphology Abnormally short growth true Inferred relationship Some 1
Brachymesophalangia Finding site Musculoskeletal structure of digit false Inferred relationship Some 1
Brachymesophalangia Finding site Phalanx structure false Inferred relationship Some 1
Brachymesophalangia Occurrence Congenital false Inferred relationship Some
Brachymesophalangia Associated morphology Developmental abnormality false Inferred relationship Some
Brachymesophalangia Associated morphology Abnormally short growth false Inferred relationship Some 1
Brachymesophalangia Occurrence Congenital false Inferred relationship Some 2
Brachymesophalangia Associated morphology Abnormally short growth false Inferred relationship Some 2
Brachymesophalangia Finding site Phalanx structure false Inferred relationship Some 2
Brachymesophalangia Occurrence Congenital true Inferred relationship Some 1
Brachymesophalangia Finding site Entire phalanx false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Sillence syndrome Is a True Brachymesophalangia Inferred relationship Some
Oral-facial-digital syndrome with short stature and brachymesophalangia Is a True Brachymesophalangia Inferred relationship Some
Brachydactyly type A4 Is a True Brachymesophalangia Inferred relationship Some
Brachydactyly type A6 Is a True Brachymesophalangia Inferred relationship Some
Cryptomicrotia, brachydactyly, excess fingertip arch syndrome Is a True Brachymesophalangia Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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