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27837003: Pyle metaphyseal dysplasia (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
46590012 Pyle metaphyseal dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
46591011 Pyle disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
196628015 Pyle's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
758450015 Pyle metaphyseal dysplasia (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
46590012 Pyle metaphyseal dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
46591011 Pyle disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
196628015 Pyle's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
483686012 Metaphyseal dysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
758450015 Pyle metaphyseal dysplasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
758450015 Pyle metaphyseal dysplasia (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3384381001000115 Pyle-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4479621000241119 dysplasie métaphysaire familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4479621000241119 dysplasie métaphysaire familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3384381001000115 Pyle-Krankheit 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
Pyle metaphyseal dysplasia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Pyle metaphyseal dysplasia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Pyle metaphyseal dysplasia Is a Dysplasia with increased bone density true Inferred relationship Existential restriction modifier (core metadata concept)
Pyle metaphyseal dysplasia Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pyle metaphyseal dysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pyle metaphyseal dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Pyle metaphyseal dysplasia Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pyle metaphyseal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pyle metaphyseal dysplasia Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Pyle metaphyseal dysplasia Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pyle metaphyseal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pyle metaphyseal dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pyle metaphyseal dysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pyle metaphyseal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pyle metaphyseal dysplasia Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pyle metaphyseal dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pyle metaphyseal dysplasia Interprets Bone density scan true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pyle metaphyseal dysplasia Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pyle metaphyseal dysplasia Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier (core metadata concept)
Pyle metaphyseal dysplasia Is a Developmental hereditary disorder 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

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