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770681000: Robin sequence and oligodactyly syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3702093019 Robin sequence and oligodactyly syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3702094013 Robin sequence and oligodactyly syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3702095014 Pierre Robin sequence, oligodactyly syndrome 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
Robin sequence and oligodactyly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Robin sequence and oligodactyly syndrome Is a Robin sequence true Inferred relationship Existential restriction modifier
Robin sequence and oligodactyly syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Robin sequence and oligodactyly syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 1
Robin sequence and oligodactyly syndrome Is a Adactyly true Inferred relationship Existential restriction modifier
Robin sequence and oligodactyly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Robin sequence and oligodactyly syndrome Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 2
Robin sequence and oligodactyly syndrome Finding site Digit structure true Inferred relationship Existential restriction modifier 2
Robin sequence and oligodactyly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Robin sequence and oligodactyly syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Robin sequence and oligodactyly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Robin sequence and oligodactyly syndrome Associated morphology Absence true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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