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49984004: FG 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
83254013 FG syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
787722011 FG syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1800901000000116 Opitz-Kaveggia syndrome en Synonym Active Entire term case sensitive SNOMED CT United Kingdom Edition module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
FG syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
FG syndrome Finding site Musculoskeletal structure of limb false Inferred relationship Existential restriction modifier
FG syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
FG syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier
FG syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
FG syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier 1
FG syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
FG syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier 1
FG syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
FG syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
FG syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
FG syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
FG syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
FG syndrome Finding site Limb structure true Inferred relationship Existential restriction modifier 2
FG syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 3
FG syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
FG syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
FG syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
FG syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
FG syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
FG syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
FG syndrome type 1 Is a True FG syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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