FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

254133005: Pachydermoperiostosis - familial (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
378305012 Pachydermoperiostosis - familial en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
378306013 Familial hypertrophic osteoarthropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644983015 Pachydermoperiostosis - familial (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
378305012 Pachydermoperiostosis - familial en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
378305012 Pachydermoperiostosis - familial en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
378306013 Familial hypertrophic osteoarthropathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
378306013 Familial hypertrophic osteoarthropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644983015 Pachydermoperiostosis - familial (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
644983015 Pachydermoperiostosis - familial (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
80951000077118 pachydermopériostose familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
80951000077118 pachydermopériostose familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pachydermoperiostosis - familial Is a Dysplasia with increased bone density true Inferred relationship Existential restriction modifier (core metadata concept)
Pachydermoperiostosis - familial Is a Multisystem disorder O-P false Inferred relationship Existential restriction modifier (core metadata concept)
Pachydermoperiostosis - familial Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pachydermoperiostosis - familial Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Pachydermoperiostosis - familial Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pachydermoperiostosis - familial Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pachydermoperiostosis - familial Is a trouble multisytémique false Inferred relationship Existential restriction modifier (core metadata concept)
Pachydermoperiostosis - familial Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pachydermoperiostosis - familial Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pachydermoperiostosis - familial Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pachydermoperiostosis - familial Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pachydermoperiostosis - familial Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pachydermoperiostosis - familial Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pachydermoperiostosis - familial Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pachydermoperiostosis - familial Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pachydermoperiostosis - familial Interprets Bone density scan true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pachydermoperiostosis - familial Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pachydermoperiostosis - familial Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start