FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  FHIR Version n/a  User: [n/a]

31925001: Hereditary factor I deficiency disease (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
485078010 Congenital afibrinogenaemia en Synonym Inactive Initial character case insensitive SNOMED CT core
485079019 Congenital hypofibrinogenaemia en Synonym Inactive Initial character case insensitive SNOMED CT core
485080016 Hereditary hypofibrinogenaemia en Synonym Active Case insensitive SNOMED CT core
53348015 Hereditary factor I deficiency disease en Synonym Active Initial character case insensitive SNOMED CT core
53349011 Hereditary factor I deficiency disease, NOS en Synonym Inactive Initial character case insensitive SNOMED CT core
53350011 Hereditary hypofibrinogenemia en Synonym Active Case insensitive SNOMED CT core
53351010 Congenital hypofibrinogenemia en Synonym Inactive Initial character case insensitive SNOMED CT core
53352015 Congenital afibrinogenemia en Synonym Inactive Initial character case insensitive SNOMED CT core
763149014 Hereditary factor I deficiency disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary factor I deficiency disease Has interpretation Abnormal true Inferred relationship Some 2
Hereditary factor I deficiency disease Interprets Haemostatic function true Inferred relationship Some 2
Hereditary factor I deficiency disease Is a Factor XIII deficiency disease false Inferred relationship Some
Hereditary factor I deficiency disease Is a Hereditary coagulation factor deficiency false Inferred relationship Some
Hereditary factor I deficiency disease Is a Congenital fibrinogen abnormality true Inferred relationship Some
Hereditary factor I deficiency disease Occurrence Congenital true Inferred relationship Some 1
Hereditary factor I deficiency disease Finding site Body system structure false Inferred relationship Some
Hereditary factor I deficiency disease Has definitional manifestation Haemostatic system finding false Inferred relationship Some
Hereditary factor I deficiency disease Is a Hereditary coagulation factor deficiency true Inferred relationship Some
Hereditary factor I deficiency disease Finding site Entire haematological system false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital hypofibrinogenaemia Is a True Hereditary factor I deficiency disease Inferred relationship Some
Hereditary dysfibrinogenaemia Is a True Hereditary factor I deficiency disease Inferred relationship Some
Congenital afibrinogenaemia Is a True Hereditary factor I deficiency disease Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start