39674000: familiaire C3b-inhibitordeficiëntie (aandoening)

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

\Genetic disease\Hereditary disease\...

\Hereditary disorder by system\Hereditary disorder of immune system\Familial C3B inhibitor deficiency syndrome

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Familial C3B inhibitor deficiency syndrome

\Disorder of immune function (disorder)\Hereditary disorder of immune system\Familial C3B inhibitor deficiency syndrome
\Disorder of immune function (disorder)\Immunodeficiency disorder\Primary immune deficiency disorder\Disorder of complement\Complement deficiency disease\Complement regulatory factor defect\Familial C3B inhibitor deficiency syndrome

\Disorder of body system\Disorder of immune structure (disorder)\Complement regulatory factor defect\Familial C3B inhibitor deficiency syndrome
\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Familial C3B inhibitor deficiency syndrome

\Familial disease\Familial C3B inhibitor deficiency syndrome

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

66901019 Familial C3B inhibitor deficiency syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
776173013 Familial C3B inhibitor deficiency syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6219531000146117 familiaire C3b-inhibitordeficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6219541000146113 familiaire C3b-inhibitordeficiëntie (aandoening) nl Fully specified name 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
Familial C3B inhibitor deficiency syndrome	Is a	Complement regulatory factor defect	true	Inferred relationship	Some
Familial C3B inhibitor deficiency syndrome	Is a	Hereditary disorder of immune system	true	Inferred relationship	Some
Familial C3B inhibitor deficiency syndrome	Is a	Familial disease	true	Inferred relationship	Some
Familial C3B inhibitor deficiency syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Familial C3B inhibitor deficiency syndrome	Finding site	Structure of immune system (body structure)	true	Inferred relationship	Some	1
Familial C3B inhibitor deficiency syndrome	Has definitional manifestation	Immune system finding	false	Inferred relationship	Some
Familial C3B inhibitor deficiency syndrome	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets