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205506004: Craniodiaphyseal 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
315143015 Craniodiaphyseal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
315144014 CDD - Craniodiaphyseal dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
590883011 Craniodiaphyseal dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
315143015 Craniodiaphyseal dysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
315143015 Craniodiaphyseal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
315144014 CDD - Craniodiaphyseal dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
590883011 Craniodiaphyseal dysplasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
590883011 Craniodiaphyseal dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3427701001000118 Dysplasie, kraniodiaphysäre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
950181000172119 dysplasie cranio-diaphysaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
950181000172119 dysplasie cranio-diaphysaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3427701001000118 Dysplasie, kraniodiaphysäre 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
Craniodiaphyseal dysplasia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Craniodiaphyseal dysplasia Is a Dysplasia with increased bone density true Inferred relationship Existential restriction modifier (core metadata concept)
Craniodiaphyseal dysplasia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Craniodiaphyseal dysplasia Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniodiaphyseal dysplasia Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniodiaphyseal dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Craniodiaphyseal dysplasia Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniodiaphyseal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniodiaphyseal dysplasia Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Craniodiaphyseal dysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniodiaphyseal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniodiaphyseal dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniodiaphyseal dysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniodiaphyseal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniodiaphyseal dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniodiaphyseal dysplasia Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniodiaphyseal dysplasia Interprets Bone density scan true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniodiaphyseal dysplasia Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniodiaphyseal dysplasia Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier (core metadata concept)
Craniodiaphyseal 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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