33297000: hereditaire stollingsfactor II-deficiëntie (aandoening)

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

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

\Prothrombin complex deficiency\Factor II deficiency\Hereditary factor II deficiency disease

\Coagulation factor deficiency syndrome\Factor II deficiency\Hereditary factor II deficiency disease
\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor II deficiency disease

\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor II deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Prothrombin complex deficiency\Factor II deficiency\Hereditary factor II deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor II deficiency\Hereditary factor II deficiency disease
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor II deficiency disease

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

Descriptions:

Id Description Lang Type Status Case? Module

55565011 Hereditary factor II deficiency disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

55566012 Hereditary hypoprothrombinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

485473013 Hereditary hypoprothrombinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

764682017 Hereditary factor II deficiency disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

345541000146114 hereditaire factor II-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

9890821000146112 hereditaire stollingsfactor II-deficiëntie (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

9892891000146114 hereditaire stollingsfactor II-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary factor II deficiency disease	Is a	Hereditary coagulation factor deficiency	true	Inferred relationship	Some
Hereditary factor II deficiency disease	Is a	Factor II deficiency	true	Inferred relationship	Some
Hereditary factor II deficiency disease	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Hereditary factor II deficiency disease	Finding site	Body system structure	false	Inferred relationship	Some
Hereditary factor II deficiency disease	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Hereditary factor II deficiency disease	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary factor II deficiency disease	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets