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770947009: Autosomal dominant severe congenital neutropenia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3703563012 Autosomal dominant severe congenital neutropaenia en Synonym Active Entire term case insensitive SNOMED CT core module
3703564018 Autosomal dominant severe congenital neutropenia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3703565017 Autosomal dominant severe congenital neutropenia en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant severe congenital neutropenia Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant severe congenital neutropenia Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Autosomal dominant severe congenital neutropenia Is a Congenital neutropenia true Inferred relationship Existential restriction modifier
Autosomal dominant severe congenital neutropenia Has interpretation Below reference range true Inferred relationship Existential restriction modifier 1
Autosomal dominant severe congenital neutropenia Interprets Neutrophil count true Inferred relationship Existential restriction modifier 1
Autosomal dominant severe congenital neutropenia Is a Hereditary cancer-predisposing syndrome true Inferred relationship Existential restriction modifier
Autosomal dominant severe congenital neutropenia Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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