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

726708009: Familial isolated congenital asplenia (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
3451940015 Familial isolated congenital asplenia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3451941016 Familial isolated congenital asplenia 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
Familial isolated congenital asplenia Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial isolated congenital asplenia Is a Congenital absence of spleen true Inferred relationship Existential restriction modifier
Familial isolated congenital asplenia Is a Familial disease true Inferred relationship Existential restriction modifier
Familial isolated congenital asplenia Is a Hereditary disorder by system true Inferred relationship Existential restriction modifier
Familial isolated congenital asplenia Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Familial isolated congenital asplenia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Familial isolated congenital asplenia Finding site Splenic structure true Inferred relationship Existential restriction modifier 1
Familial isolated congenital asplenia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Familial isolated congenital asplenia Is a Asplenia false Inferred relationship Existential restriction modifier
Familial isolated congenital asplenia Is a Aplasia of spleen false Inferred relationship Existential restriction modifier
Familial isolated congenital asplenia Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Familial isolated congenital asplenia Associated morphology Absence true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start