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1162837001: Proximal interphalangeal joint symphalangism Cushing type (disorder)


Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4591705016 Symphalangism Cushing type en Synonym Active Initial character case insensitive SNOMED CT core
4591708019 Proximal interphalangeal joint symphalangism Cushing type (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
4591709010 Proximal interphalangeal joint symphalangism Cushing type en Synonym Active Initial character case insensitive SNOMED CT core
4591707012 A very rare genetic bone disorder with characteristics of ankylosis of the proximal interphalangeal joints, carpal and tarsal bone fusion, and conductive hearing loss in some patients. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Symphalangism Cushing type Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Symphalangism Cushing type Is a Proximal interphalangeal joint symphalangism true Inferred relationship Some
Symphalangism Cushing type Is a Developmental hereditary disorder true Inferred relationship Some
Symphalangism Cushing type Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Symphalangism Cushing type Occurrence Congenital true Inferred relationship Some 1
Symphalangism Cushing type Finding site Structure of proximal interphalangeal joint of digit true Inferred relationship Some 1
Symphalangism Cushing type Associated morphology Ankylosis true Inferred relationship Some 1
Symphalangism Cushing type Pathological process Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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