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782689003: Congenital pseudoarthrosis of limb (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3755222010 Congenital pseudoarthrosis of limb (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3755223017 Congenital pseudoarthrosis of limb en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3755224011 A rare genetic non-syndromic limb malformation with characteristics of delayed union or non-union of a long bone, resulting in formation of a false joint, with abnormal mobility and angulation at the pseudoarthrosis site, which manifests with progressive anterolateral forearm or leg bowing, limb shortening, and non-healing fractures. Typical histopathological findings include fibromatosis-like proliferation in the soft tissues with cystic or dysplastic lesions. Neurofibromatosis and osteofibrous dysplasia are frequently associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3755222010 Congenital pseudoarthrosis of limb (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3755223017 Congenital pseudoarthrosis of limb en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3755224011 A rare genetic non-syndromic limb malformation with characteristics of delayed union or non-union of a long bone, resulting in formation of a false joint, with abnormal mobility and angulation at the pseudoarthrosis site, which manifests with progressive anterolateral forearm or leg bowing, limb shortening, and non-healing fractures. Typical histopathological findings include fibromatosis-like proliferation in the soft tissues with cystic or dysplastic lesions. Neurofibromatosis and osteofibrous dysplasia are frequently associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
1055121000195111 Pseudoarthrose der Gliedmassen, kongenitale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5906061000241113 pseudoarthrose congénitale d'un membre fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5906061000241113 pseudoarthrose congénitale d'un membre fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1055121000195111 Pseudoarthrose der Gliedmassen, kongenitale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3453421001000113 Pseudoarthrose der Gliedmaßen, kongenitale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital pseudoarthrosis of limb (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pseudoarthrosis of limb (disorder) Finding site Bone structure of extremity true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pseudoarthrosis of limb (disorder) Is a Congenital anomaly of limb true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pseudoarthrosis of limb (disorder) Associated morphology Congenital pseudoarthrosis false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pseudoarthrosis of limb (disorder) Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pseudoarthrosis of limb (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pseudoarthrosis of limb (disorder) Is a Pseudoarthrosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pseudoarthrosis of limb (disorder) Associated morphology Pseudoarthrosis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital pseudoarthrosis of limb (disorder) Is a Genetic disease true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital pseudoarthrosis of tibia (disorder) Is a True Congenital pseudoarthrosis of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pseudoarthrosis of clavicle (disorder) Is a True Congenital pseudoarthrosis of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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