FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

725137007: Neutropenia, monocytopenia, deafness syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3487932011 Neutropenia, monocytopenia, deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3487933018 Neutropenia, monocytopenia, deafness syndrome 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
Neutropenia, monocytopenia, deafness syndrome Is a Congenital immunodeficiency disease false Inferred relationship Existential restriction modifier
Neutropenia, monocytopenia, deafness syndrome Is a Congenital deafness true Inferred relationship Existential restriction modifier
Neutropenia, monocytopenia, deafness syndrome Is a Hearing loss associated with syndrome true Inferred relationship Existential restriction modifier
Neutropenia, monocytopenia, deafness syndrome Is a Neutropenic disorder false Inferred relationship Existential restriction modifier
Neutropenia, monocytopenia, deafness syndrome Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier
Neutropenia, monocytopenia, deafness syndrome Has definitional manifestation Neutropenia false Inferred relationship Existential restriction modifier
Neutropenia, monocytopenia, deafness syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Neutropenia, monocytopenia, deafness syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Neutropenia, monocytopenia, deafness syndrome Finding site Inner ear structure false Inferred relationship Existential restriction modifier 3
Neutropenia, monocytopenia, deafness syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 1
Neutropenia, monocytopenia, deafness syndrome Interprets Neutrophil count true Inferred relationship Existential restriction modifier 1
Neutropenia, monocytopenia, deafness syndrome Is a Neutropenia false Inferred relationship Existential restriction modifier
Neutropenia, monocytopenia, deafness syndrome Finding site Inner ear structure true Inferred relationship Existential restriction modifier 2
Neutropenia, monocytopenia, deafness syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Neutropenia, monocytopenia, deafness syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Neutropenia, monocytopenia, deafness syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Neutropenia, monocytopenia, deafness syndrome Is a Congenital neutropenia true Inferred relationship Existential restriction modifier
Neutropenia, monocytopenia, deafness syndrome Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 3
Neutropenia, monocytopenia, deafness syndrome Is a Congenital anomaly of ear with impairment of hearing true Inferred relationship Existential restriction modifier
Neutropenia, monocytopenia, deafness syndrome Is a Congenital anomaly of inner ear true Inferred relationship Existential restriction modifier
Neutropenia, monocytopenia, deafness syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start