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721873007: orofaciodigitaal syndroom type 6 (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
3326396016 Joubert syndrome with orofaciodigital defect (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3326397013 Joubert syndrome with orofaciodigital defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3326398015 Joubert syndrome with oro-facial-digital syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3326399011 Orofaciodigital syndrome type 6 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326400016 Varadi Papp syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3326401017 Varadi syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6093241000146119 orofaciodigitaal syndroom type 6 (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6093251000146116 orofaciodigitaal syndroom type 6 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6093261000146118 syndroom van Joubert met orofaciodigitaal defect nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6848041000146113 syndroom van Váradi nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6848051000146111 syndroom van Váradi-Papp nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6848061000146114 OFD6 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3326402012 A very rare subtype of Joubert syndrome and related disorders with characteristics of neurological features of Joubert syndrome associated with orofacial anomalies and often polydactyly. Prevalence is unknown. Typical oral findings include bifid or lobulated tongue, lingual hamartomas and multiple oral frenula, but cleft lip and/or palate can also be present. Two OFD6 patients, including one fetus, were found to carry a homozygous mutation in the TMEM216 gene (11q13.1), but mutations in this gene were excluded in several other patients and the genetic basis of this condition still remains elusive. 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 orofaciodigital defect (disorder) Is a Oral-facial-digital syndrome true Inferred relationship Some
Joubert syndrome with orofaciodigital defect (disorder) Is a Hereditary disorder of the integument true Inferred relationship Some
Joubert syndrome with orofaciodigital defect (disorder) Is a Joubert syndrome (disorder) true Inferred relationship Some
Joubert syndrome with orofaciodigital defect (disorder) Occurrence Congenital true Inferred relationship Some 5
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 6
Joubert syndrome with orofaciodigital defect (disorder) Occurrence Congenital true Inferred relationship Some 6
Joubert syndrome with orofaciodigital defect (disorder) Occurrence Congenital false Inferred relationship Some 7
Joubert syndrome with orofaciodigital defect (disorder) Occurrence Congenital false Inferred relationship Some 8
Joubert syndrome with orofaciodigital defect (disorder) Occurrence Congenital false Inferred relationship Some 9
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 5
Joubert syndrome with orofaciodigital defect (disorder) Finding site Limb structure false Inferred relationship Some 5
Joubert syndrome with orofaciodigital defect (disorder) Finding site Skin structure true Inferred relationship Some 5
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 7
Joubert syndrome with orofaciodigital defect (disorder) Finding site Ectoderm structure false Inferred relationship Some 7
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 9
Joubert syndrome with orofaciodigital defect (disorder) Finding site Face structure false Inferred relationship Some 6
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology Aplasia false Inferred relationship Some 8
Joubert syndrome with orofaciodigital defect (disorder) Finding site Cerebellar vermis structure false Inferred relationship Some 8
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 6
Joubert syndrome with orofaciodigital defect (disorder) Finding site Ectoderm structure true Inferred relationship Some 6
Joubert syndrome with orofaciodigital defect (disorder) Finding site Skin structure false Inferred relationship Some 9
Joubert syndrome with orofaciodigital defect (disorder) Is a Digestive system hereditary disorder (disorder) true Inferred relationship Some
Joubert syndrome with orofaciodigital defect (disorder) Occurrence Congenital true Inferred relationship Some 1
Joubert syndrome with orofaciodigital defect (disorder) Occurrence Congenital true Inferred relationship Some 2
Joubert syndrome with orofaciodigital defect (disorder) Finding site Structure of internal part of mouth true Inferred relationship Some 2
Joubert syndrome with orofaciodigital defect (disorder) Occurrence Congenital true Inferred relationship Some 4
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 4
Joubert syndrome with orofaciodigital defect (disorder) Finding site Digit structure true Inferred relationship Some 4
Joubert syndrome with orofaciodigital defect (disorder) Occurrence Congenital true Inferred relationship Some 3
Joubert syndrome with orofaciodigital defect (disorder) Finding site Structure of internal part of mouth false Inferred relationship Some 4
Joubert syndrome with orofaciodigital defect (disorder) Finding site Digit structure false Inferred relationship Some 5
Joubert syndrome with orofaciodigital defect (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 4
Joubert syndrome with orofaciodigital defect (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology Aplasia true Inferred relationship Some 1
Joubert syndrome with orofaciodigital defect (disorder) Finding site Cerebellar vermis structure true Inferred relationship Some 1
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Joubert syndrome with orofaciodigital defect (disorder) Finding site Face structure true Inferred relationship Some 3
Joubert syndrome with orofaciodigital defect (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 5
Joubert syndrome with orofaciodigital defect (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 5
Joubert syndrome with orofaciodigital defect (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Joubert syndrome with orofaciodigital defect (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 6
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Joubert syndrome with orofaciodigital defect (disorder) Associated morphology Dysplasia true Inferred relationship Some 6

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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