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62803002: Frontometaphyseal dysplasia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
104373017 Frontometaphyseal dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module
802016016 Frontometaphyseal dysplasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1232394014 FMD - Frontometaphyseal dysplasia en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Frontometaphyseal dysplasia Is a Osteochondrodysplasia syndrome true Inferred relationship Existential restriction modifier
Frontometaphyseal dysplasia Is a Dysplasia with increased bone density true Inferred relationship Existential restriction modifier
Frontometaphyseal dysplasia Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Frontometaphyseal dysplasia Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
Frontometaphyseal dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier
Frontometaphyseal dysplasia Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Frontometaphyseal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Frontometaphyseal dysplasia Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Frontometaphyseal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Frontometaphyseal dysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier 1
Frontometaphyseal dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Frontometaphyseal dysplasia Finding site Bone structure false Inferred relationship Existential restriction modifier 2
Frontometaphyseal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Frontometaphyseal dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Frontometaphyseal dysplasia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Frontometaphyseal dysplasia Interprets Bone density scan true Inferred relationship Existential restriction modifier 2
Frontometaphyseal dysplasia Has interpretation Above reference range true Inferred relationship Existential restriction modifier 2
Frontometaphyseal dysplasia Is a Otopalatodigital syndrome spectrum disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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