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1162837001: Proximal interphalangeal joint symphalangism Cushing type (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4591705016 Symphalangism Cushing type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4591708019 Proximal interphalangeal joint symphalangism Cushing type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4591709010 Proximal interphalangeal joint symphalangism Cushing type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5399278015 A rare genetic bone disorder characterized by ankylosis of the proximal interphalangeal joints, carpal and tarsal bone fusion, and conductive hearing loss in some patients. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399279011 A rare genetic bone disorder characterised by ankylosis of the proximal interphalangeal joints, carpal and tarsal bone fusion, and conductive hearing loss in some patients. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4591705016 Symphalangism Cushing type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4591708019 Proximal interphalangeal joint symphalangism Cushing type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4591709010 Proximal interphalangeal joint symphalangism Cushing type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core
5399278015 A rare genetic bone disorder characterized by ankylosis of the proximal interphalangeal joints, carpal and tarsal bone fusion, and conductive hearing loss in some patients. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399279011 A rare genetic bone disorder characterised by ankylosis of the proximal interphalangeal joints, carpal and tarsal bone fusion, and conductive hearing loss in some patients. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
652111000274119 Symphalangismus des proximalen Interphalangealgelenks Typ Cushing de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
652111000274119 Symphalangismus des proximalen Interphalangealgelenks Typ Cushing de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3455251001000119 Symphalangismus, proximaler de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Proximal interphalangeal joint symphalangism Cushing type (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Proximal interphalangeal joint symphalangism Cushing type (disorder) Is a Proximal interphalangeal joint symphalangism true Inferred relationship Existential restriction modifier (core metadata concept)
Proximal interphalangeal joint symphalangism Cushing type (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Proximal interphalangeal joint symphalangism Cushing type (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Proximal interphalangeal joint symphalangism Cushing type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Proximal interphalangeal joint symphalangism Cushing type (disorder) Finding site Structure of proximal interphalangeal joint of digit true Inferred relationship Existential restriction modifier (core metadata concept) 1
Proximal interphalangeal joint symphalangism Cushing type (disorder) Associated morphology Ankylosis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Proximal interphalangeal joint symphalangism Cushing type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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