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770947009: autosomaal dominante ernstige congenitale neutropenie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3703563012 Autosomal dominant severe congenital neutropaenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3703564018 Autosomal dominant severe congenital neutropenia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3703565017 Autosomal dominant severe congenital neutropenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6353531000146118 autosomaal dominante ernstige congenitale neutropenie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6353541000146114 autosomaal dominante ernstige congenitale neutropenie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6353551000146112 autosomaal dominante ernstige aangeboren neutrocytopenie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3703566016 A rare primary immunodeficiency disorder with characteristics of autosomal dominant inheritance, absolute neutrophil counts below 0.5x10E9/L in the peripheral blood (on three separate occasions over a six month period), granulopoiesis maturation arrest at the promyelocyte/myelocyte stage and early-onset severe recurrent bacterial infections. 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
Autosomal dominant severe congenital neutropaenia Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant severe congenital neutropaenia Occurrence Congenital true Inferred relationship Some 2
Autosomal dominant severe congenital neutropaenia Is a Congenital neutropenia true Inferred relationship Some
Autosomal dominant severe congenital neutropaenia Has interpretation Below reference range true Inferred relationship Some 1
Autosomal dominant severe congenital neutropaenia Interprets Neutrophil count true Inferred relationship Some 1
Autosomal dominant severe congenital neutropaenia Is a Hereditary cancer-predisposing syndrome true Inferred relationship Some
Autosomal dominant severe congenital neutropaenia Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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