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719689005: Multiple epiphyseal dysplasia Beighton type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3317497018 Multiple epiphyseal dysplasia Beighton type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3317498011 Multiple epiphyseal dysplasia Beighton type en Synonym Active Only initial character case insensitive SNOMED CT core module
3317499015 Multiple epiphyseal dysplasia with myopia and deafness syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multiple epiphyseal dysplasia Beighton type Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Multiple epiphyseal dysplasia Beighton type Is a Multiple epiphyseal dysplasia true Inferred relationship Existential restriction modifier
Multiple epiphyseal dysplasia Beighton type Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Multiple epiphyseal dysplasia Beighton type Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Multiple epiphyseal dysplasia Beighton type Finding site Structure of epiphysis false Inferred relationship Existential restriction modifier 2
Multiple epiphyseal dysplasia Beighton type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Multiple epiphyseal dysplasia Beighton type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Multiple epiphyseal dysplasia Beighton type Finding site Structure of epiphysis true Inferred relationship Existential restriction modifier 1
Multiple epiphyseal dysplasia Beighton type Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Multiple epiphyseal dysplasia Beighton type Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Multiple epiphyseal dysplasia Beighton type Clinical course Progressive true Inferred relationship Existential restriction modifier 2
Multiple epiphyseal dysplasia Beighton type Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Multiple epiphyseal dysplasia Beighton type Has interpretation Decreased true Inferred relationship Existential restriction modifier 3
Multiple epiphyseal dysplasia Beighton type Finding site Ear structure true Inferred relationship Existential restriction modifier 4
Multiple epiphyseal dysplasia Beighton type Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Multiple epiphyseal dysplasia Beighton type Is a Chronic disease of ear false Inferred relationship Existential restriction modifier
Multiple epiphyseal dysplasia Beighton type Interprets Hearing, function true Inferred relationship Existential restriction modifier 3
Multiple epiphyseal dysplasia Beighton type Is a Congenital conductive hearing loss true Inferred relationship Existential restriction modifier
Multiple epiphyseal dysplasia Beighton type Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 4
Multiple epiphyseal dysplasia Beighton type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Multiple epiphyseal dysplasia Beighton type Interprets Height / growth measure true Inferred relationship Existential restriction modifier 5
Multiple epiphyseal dysplasia Beighton type Is a Chronic deafness 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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