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50913002: Grob's syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2841975017 Grob syndrome en Synonym Active Case sensitive SNOMED CT core
788754017 Grob's syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
84831018 Grob's syndrome en Synonym Active Case sensitive SNOMED CT core
84832013 Dysplasia linguofacialis syndrome en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Grob's syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Grob's syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Grob's syndrome Associated morphology Congenital malformation false Inferred relationship Some
Grob's syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Grob's syndrome Occurrence Congenital true Inferred relationship Some 1
Grob's syndrome Associated morphology Developmental abnormality false Inferred relationship Some 1
Grob's syndrome Finding site Face structure true Inferred relationship Some 1
Grob's syndrome Occurrence Congenital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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