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

721847002: Joubert syndrome with congenital hepatic fibrosis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3326243010 Joubert syndrome with congenital hepatic fibrosis (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3326244016 Joubert syndrome with hepatic defect en Synonym Active Entire term case sensitive SNOMED CT core module
3326245015 Joubert syndrome with congenital hepatic fibrosis en Synonym Active Entire term case sensitive SNOMED CT core module
3326246019 Cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis en Synonym Active Entire term case insensitive SNOMED CT core module
3326247011 COACH syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3326248018 Gentile syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3326250014 COACH (cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Joubert syndrome with congenital hepatic fibrosis Is a Congenital hepatic fibrosis true Inferred relationship Existential restriction modifier
Joubert syndrome with congenital hepatic fibrosis Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Joubert syndrome with congenital hepatic fibrosis Is a Joubert syndrome true Inferred relationship Existential restriction modifier
Joubert syndrome with congenital hepatic fibrosis Associated morphology Aplasia false Inferred relationship Existential restriction modifier 2
Joubert syndrome with congenital hepatic fibrosis Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Joubert syndrome with congenital hepatic fibrosis Finding site Cerebellar vermis structure false Inferred relationship Existential restriction modifier 2
Joubert syndrome with congenital hepatic fibrosis Associated morphology Fibrosis false Inferred relationship Existential restriction modifier 3
Joubert syndrome with congenital hepatic fibrosis Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Joubert syndrome with congenital hepatic fibrosis Finding site Liver structure false Inferred relationship Existential restriction modifier 3
Joubert syndrome with congenital hepatic fibrosis Associated morphology Fibrosis true Inferred relationship Existential restriction modifier 2
Joubert syndrome with congenital hepatic fibrosis Finding site Liver structure true Inferred relationship Existential restriction modifier 2
Joubert syndrome with congenital hepatic fibrosis Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Joubert syndrome with congenital hepatic fibrosis Finding site Cerebellar vermis structure true Inferred relationship Existential restriction modifier 1
Joubert syndrome with congenital hepatic fibrosis Associated morphology Aplasia true Inferred relationship Existential restriction modifier 1
Joubert syndrome with congenital hepatic fibrosis Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Joubert syndrome with congenital hepatic fibrosis Is a Congenital anomaly of liver false Inferred relationship Existential restriction modifier
Joubert syndrome with congenital hepatic fibrosis Occurrence Congenital 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