FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

427167008: hereditair angio-oedeem type III (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2007. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2674272018 Hereditary angioneurotic oedema with normal C1 esterase inhibitor activity en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2674273011 Hereditary angioedema - type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2674274017 Hereditary angio-oedema with normal C1 esterase inhibitor activity en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2674275016 Hereditary angioedema with normal C1 esterase inhibitor activity en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2674276015 Hereditary angioneurotic edema with normal C1 esterase inhibitor activity en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009485015 Hereditary angioedema with normal C1 esterase inhibitor activity (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
696261000146118 hereditair angio-oedeem type III (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
696271000146112 hereditair angio-oedeem type III nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3943437016 Hereditary angioedema without abnormal C1 inhibitor levels or function. One type has been found mostly in females in which symptoms may be triggered by pregnancy or estrogen-containing oral contraceptives. Mechanisms include mutations of the genes encoding coagulation factor XII, angiopoietin-1, plasminogen and as yet undefined factors. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary angioedema with normal C1 esterase inhibitor activity Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary angioedema with normal C1 esterase inhibitor activity Is a Hereditary disorder of immune system false Inferred relationship Some
Hereditary angioedema with normal C1 esterase inhibitor activity Is a Disorder of immune structure (disorder) false Inferred relationship Some
Hereditary angioedema with normal C1 esterase inhibitor activity Is a Angioedema false Inferred relationship Some
Hereditary angioedema with normal C1 esterase inhibitor activity Finding site Structure of immune system (body structure) false Inferred relationship Some 1
Hereditary angioedema with normal C1 esterase inhibitor activity Has definitional manifestation Immune system finding false Inferred relationship Some
Hereditary angioedema with normal C1 esterase inhibitor activity Associated morphology Urticaria false Inferred relationship Some 2
Hereditary angioedema with normal C1 esterase inhibitor activity Is a Hereditary angioedema true Inferred relationship Some
Hereditary angioedema with normal C1 esterase inhibitor activity Pathological process (attribute) Abnormal immune process (qualifier value) false Inferred relationship Some 3
Hereditary angioedema with normal C1 esterase inhibitor activity Associated morphology Angioedema true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start