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717337001: Syndromic hypoplasia of orbital border (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3309097011 Syndromic hypoplasia of orbital border (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3309098018 Syndromic orbital border hypoplasia en Synonym Active Entire term case insensitive SNOMED CT core module
3309099014 Urrets Zavalia syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3309100018 Syndromic hypoplasia of orbital border 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
Syndromic hypoplasia of orbital border Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Syndromic hypoplasia of orbital border Is a Congenital anomaly of orbit proper true Inferred relationship Existential restriction modifier
Syndromic hypoplasia of orbital border Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Syndromic hypoplasia of orbital border Is a Orbital margin finding true Inferred relationship Existential restriction modifier
Syndromic hypoplasia of orbital border Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Syndromic hypoplasia of orbital border Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Syndromic hypoplasia of orbital border Finding site Face structure true Inferred relationship Existential restriction modifier 2
Syndromic hypoplasia of orbital border Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Syndromic hypoplasia of orbital border Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 2
Syndromic hypoplasia of orbital border Finding site Orbital margin structure false Inferred relationship Existential restriction modifier 2
Syndromic hypoplasia of orbital border Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Syndromic hypoplasia of orbital border Finding site Face structure false Inferred relationship Existential restriction modifier 3
Syndromic hypoplasia of orbital border Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Syndromic hypoplasia of orbital border Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Syndromic hypoplasia of orbital border Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 1
Syndromic hypoplasia of orbital border Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Syndromic hypoplasia of orbital border Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Syndromic hypoplasia of orbital border Finding site Orbital margin structure true Inferred relationship Existential restriction modifier 1
Syndromic hypoplasia of orbital border Is a Developmental hereditary 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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