FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

40145002: Congenital neutrophil actin dysfunction (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
63729015 Congenital neutrophil actin dysfunction en Synonym Active Entire term case insensitive SNOMED CT core module
63730013 Actin dysfunction syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
776732016 Congenital neutrophil actin dysfunction (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital neutrophil actin dysfunction Is a Disorder of neutrophils true Inferred relationship Existential restriction modifier
Congenital neutrophil actin dysfunction Is a Qualitative abnormality of granulocyte true Inferred relationship Existential restriction modifier
Congenital neutrophil actin dysfunction Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Congenital neutrophil actin dysfunction Finding site Leukocyte false Inferred relationship Existential restriction modifier
Congenital neutrophil actin dysfunction Finding site Structure of immune system false Inferred relationship Existential restriction modifier
Congenital neutrophil actin dysfunction Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier
Congenital neutrophil actin dysfunction Associated morphology White blood cell abnormality false Inferred relationship Existential restriction modifier
Congenital neutrophil actin dysfunction Is a Congenital anomaly of the hematopoietic system false Inferred relationship Existential restriction modifier
Congenital neutrophil actin dysfunction Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital neutrophil actin dysfunction Is a Congenital disease true Inferred relationship Existential restriction modifier
Congenital neutrophil actin dysfunction Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier
Congenital neutrophil actin dysfunction Has definitional manifestation White blood cell finding false Inferred relationship Existential restriction modifier
Congenital neutrophil actin dysfunction Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier
Congenital neutrophil actin dysfunction Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start