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48180002: Otocephalic syndrome (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
80275016 Otocephalic syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
80276015 Otocephaly en Synonym Active Entire term case insensitive SNOMED CT core module
80277012 Otocephalus en Synonym Active Entire term case insensitive SNOMED CT core module
785719013 Otocephalic syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Otocephalic syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Otocephalic syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Otocephalic syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Otocephalic syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Otocephalic syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Otocephalic syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 1
Otocephalic syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Otocephalic syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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