FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

31925001: Hereditary factor I deficiency disease (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
53348015 Hereditary factor I deficiency disease en Synonym Active Only initial character case insensitive SNOMED CT core module
53350011 Hereditary hypofibrinogenemia en Synonym Active Entire term case insensitive SNOMED CT core module
485080016 Hereditary hypofibrinogenaemia en Synonym Active Entire term case insensitive SNOMED CT core module
763149014 Hereditary factor I deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary factor I deficiency disease Is a Hereditary coagulation factor deficiency false Inferred relationship Existential restriction modifier
Hereditary factor I deficiency disease Is a Congenital fibrinogen abnormality true Inferred relationship Existential restriction modifier
Hereditary factor I deficiency disease Finding site Entire hematological system false Inferred relationship Existential restriction modifier
Hereditary factor I deficiency disease Is a Factor XIII deficiency disease false Inferred relationship Existential restriction modifier
Hereditary factor I deficiency disease Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hereditary factor I deficiency disease Finding site Body system structure false Inferred relationship Existential restriction modifier
Hereditary factor I deficiency disease Has definitional manifestation Hemostatic system finding false Inferred relationship Existential restriction modifier
Hereditary factor I deficiency disease Is a Hereditary coagulation factor deficiency true Inferred relationship Existential restriction modifier
Hereditary factor I deficiency disease Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Hereditary factor I deficiency disease Interprets Hemostatic function true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital hypofibrinogenemia Is a True Hereditary factor I deficiency disease Inferred relationship Existential restriction modifier
Hereditary dysfibrinogenemia Is a True Hereditary factor I deficiency disease Inferred relationship Existential restriction modifier
Congenital afibrinogenemia Is a True Hereditary factor I deficiency disease Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start