FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

721847002: cerebellaire-vermis-agenesiesyndroom met congenitale leverfibrose (aandoening)


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

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 (core metadata concept) SNOMED CT core
3326244016 Joubert syndrome with hepatic defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3326245015 Joubert syndrome with congenital hepatic fibrosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3326246019 Cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326247011 COACH syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3326248018 Gentile syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3326250014 COACH (cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6455451000146117 syndroom van Joubert met congenitale leverfibrose nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6957281000146115 cerebellaire-vermis-agenesiesyndroom met congenitale leverfibrose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6957291000146118 joubertsyndroom met congenitale leverfibrose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6957301000146119 cerebellaire-vermis-agenesiesyndroom met congenitale leverfibrose (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3326249014 A very rare subtype of Joubert syndrome with the neurological features of Joubert Syndrome and congenital hepatic fibrosis. Prevalence is unknown. The age of onset and severity of hepatic manifestations are variable. Some patients may also present chorioretinal or optic nerve colobomas and nephronophthisis but these are not mandatory features. Over 70% of cases are due to mutations in the TMEM67 gene (8q22.1). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start