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31925001: hereditaire stollingsfactor I-deficiëntie (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\...

\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease

\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease

\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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	Some
Hereditary factor I deficiency disease	Is a	Congenital fibrinogen abnormality	true	Inferred relationship	Some
Hereditary factor I deficiency disease	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Hereditary factor I deficiency disease	Is a	Factor XIII deficiency disease	false	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	Hemostatic 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	Has interpretation	Abnormal	true	Inferred relationship	Some	2
Hereditary factor I deficiency disease	Interprets	Hemostatic function	true	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital hypofibrinogenemia (disorder)	Is a	True	Hereditary factor I deficiency disease	Inferred relationship	Some
Hereditary dysfibrinogenemia (disorder)	Is a	True	Hereditary factor I deficiency disease	Inferred relationship	Some
Congenital afibrinogenaemia	Is a	True	Hereditary factor I deficiency disease	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
53348015	Hereditary factor I deficiency disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
53350011	Hereditary hypofibrinogenemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
485080016	Hereditary hypofibrinogenaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
763149014	Hereditary factor I deficiency disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3646731000146119	erfelijke fibrinogeendeficiëntie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8720411000146110	hereditaire factor I-deficiëntie	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9890801000146116	hereditaire stollingsfactor I-deficiëntie (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9892881000146112	hereditaire stollingsfactor I-deficiëntie	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)