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721847002: Joubert syndrome with congenital hepatic fibrosis (disorder)


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
5402712010 Joubert syndrome with hepatic defect is a very rare subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with congenital hepatic fibrosis (CHF). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402713017 Joubert syndrome with hepatic defect is a very rare subtype of Joubert syndrome and related disorders characterised by the neurological features of JS associated with congenital hepatic fibrosis (CHF). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
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 Only initial character case insensitive (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
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
5402712010 Joubert syndrome with hepatic defect is a very rare subtype of Joubert syndrome and related disorders characterized by the neurological features of JS associated with congenital hepatic fibrosis (CHF). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402713017 Joubert syndrome with hepatic defect is a very rare subtype of Joubert syndrome and related disorders characterised by the neurological features of JS associated with congenital hepatic fibrosis (CHF). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3440481001000115 Joubert-Syndrom mit hepatischem Defekt de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6366871000241116 syndrome de Gentile fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6366881000241119 syndrome d'hypoplasie du vermis cérébelleux, oligophrénie, ataxie congénitale, colobome et fibrose hépatique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6366891000241117 syndrome de Joubert avec fibrose hépatique congénitale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6366871000241116 syndrome de Gentile fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6366881000241119 syndrome d'hypoplasie du vermis cérébelleux, oligophrénie, ataxie congénitale, colobome et fibrose hépatique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6366891000241117 syndrome de Joubert avec fibrose hépatique congénitale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3440481001000115 Joubert-Syndrom mit hepatischem Defekt de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


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 Existential restriction modifier (core metadata concept)
Joubert syndrome with congenital hepatic fibrosis (disorder) Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Joubert syndrome with congenital hepatic fibrosis (disorder) Is a Joubert syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Joubert syndrome with congenital hepatic fibrosis (disorder) Associated morphology Aplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with congenital hepatic fibrosis (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with congenital hepatic fibrosis (disorder) Finding site Cerebellar vermis structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with congenital hepatic fibrosis (disorder) Associated morphology Fibrosis (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Joubert syndrome with congenital hepatic fibrosis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Joubert syndrome with congenital hepatic fibrosis (disorder) Finding site Liver structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Joubert syndrome with congenital hepatic fibrosis (disorder) Associated morphology Fibrosis (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with congenital hepatic fibrosis (disorder) Finding site Liver structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with congenital hepatic fibrosis (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Joubert syndrome with congenital hepatic fibrosis (disorder) Finding site Cerebellar vermis structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Joubert syndrome with congenital hepatic fibrosis (disorder) Associated morphology Aplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Joubert syndrome with congenital hepatic fibrosis (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Joubert syndrome with congenital hepatic fibrosis (disorder) Is a Congenital anomaly of liver false Inferred relationship Existential restriction modifier (core metadata concept)
Joubert syndrome with congenital hepatic fibrosis (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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