FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.8.2 | FHIR Version n/a User: [n/a]

56604005: Cohen syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module

795135010 Cohen syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core

94131019 Cohen syndrome en Synonym Active Case sensitive SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cohen syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Some	1
Cohen syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Cohen syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Cohen syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Some
Cohen syndrome	Is a	Multiple malformation syndrome with unusual brain and/or neuromuscular findings	true	Inferred relationship	Some
Cohen syndrome	Is a	Hereditary disorder of nervous system	false	Inferred relationship	Some
Cohen syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Cohen syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Cohen syndrome	Associated morphology	Developmental abnormality	false	Inferred relationship	Some	1
Cohen syndrome	Occurrence	Congenital	false	Inferred relationship	Some
Cohen syndrome	Finding site	Brain structure	false	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Periodontitis co-occurrent with Cohen syndrome	Is a	False	Cohen syndrome	Inferred relationship	Some

Reference Sets

Australian emergency department reference set