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722106001: orofaciodigitaal syndroom type 8 (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
3330712015 Oro-facial digital syndrome type 8 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330713013 Oro-facial digital syndrome type 8 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330714019 Orofaciodigital syndrome type 8 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330715018 Oral-facial-digital syndrome Edwards type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3330716017 Orofaciodigital syndrome Edwards type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6801791000146117 orofaciodigitaal syndroom type 8 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6801801000146118 orofaciodigitaal syndroom type 8 (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6845691000146115 orofaciodigitaal syndroom Edwards-type nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6942711000146117 OFD8 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3330717014 Syndrome with characteristics of tongue lobulation, hypoplasia of the epiglottis, median cleft upper lip, broad or bifid nasal tip, hypertelorism or telecanthus, bilateral preaxial and postaxial polydactyly, abnormal tibia and/or radius, duplication of the halluces, short stature and mild intellectual deficit. The syndrome has been described in one family with four affected males in three generations. Increased susceptibility to respiratory infections has been noted. X-linked recessive transmission has been suggested, but the causative gene has not yet been identified. 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
Oro-facial digital syndrome type 8 (disorder) Is a Oral-facial-digital syndrome true Inferred relationship Some
Oro-facial digital syndrome type 8 (disorder) Is a mentale retardatie false Inferred relationship Some
Oro-facial digital syndrome type 8 (disorder) Is a X-linked hereditary disease false Inferred relationship Some
Oro-facial digital syndrome type 8 (disorder) Is a Hereditary disorder of the integument true Inferred relationship Some
Oro-facial digital syndrome type 8 (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 4
Oro-facial digital syndrome type 8 (disorder) Occurrence Congenital true Inferred relationship Some 4
Oro-facial digital syndrome type 8 (disorder) Finding site Face structure false Inferred relationship Some 4
Oro-facial digital syndrome type 8 (disorder) Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 5
Oro-facial digital syndrome type 8 (disorder) Occurrence Congenital true Inferred relationship Some 5
Oro-facial digital syndrome type 8 (disorder) Finding site Ectoderm structure true Inferred relationship Some 5
Oro-facial digital syndrome type 8 (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 6
Oro-facial digital syndrome type 8 (disorder) Occurrence Congenital false Inferred relationship Some 6
Oro-facial digital syndrome type 8 (disorder) Occurrence Congenital false Inferred relationship Some 7
Oro-facial digital syndrome type 8 (disorder) Finding site Skin structure true Inferred relationship Some 4
Oro-facial digital syndrome type 8 (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 5
Oro-facial digital syndrome type 8 (disorder) Finding site Limb structure false Inferred relationship Some 6
Oro-facial digital syndrome type 8 (disorder) Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 7
Oro-facial digital syndrome type 8 (disorder) Finding site Ectoderm structure false Inferred relationship Some 7
Oro-facial digital syndrome type 8 (disorder) Finding site Skin structure false Inferred relationship Some 5
Oro-facial digital syndrome type 8 (disorder) Is a Intellectual disability true Inferred relationship Some
Oro-facial digital syndrome type 8 (disorder) Is a Digestive system hereditary disorder (disorder) true Inferred relationship Some
Oro-facial digital syndrome type 8 (disorder) Occurrence Congenital true Inferred relationship Some 1
Oro-facial digital syndrome type 8 (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 2
Oro-facial digital syndrome type 8 (disorder) Occurrence Congenital true Inferred relationship Some 2
Oro-facial digital syndrome type 8 (disorder) Finding site Structure of internal part of mouth true Inferred relationship Some 1
Oro-facial digital syndrome type 8 (disorder) Finding site Digit structure false Inferred relationship Some 2
Oro-facial digital syndrome type 8 (disorder) Finding site Digit structure true Inferred relationship Some 3
Oro-facial digital syndrome type 8 (disorder) Occurrence Congenital true Inferred relationship Some 3
Oro-facial digital syndrome type 8 (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
Oro-facial digital syndrome type 8 (disorder) Finding site Structure of internal part of mouth false Inferred relationship Some 3
Oro-facial digital syndrome type 8 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Oro-facial digital syndrome type 8 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Oro-facial digital syndrome type 8 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Oro-facial digital syndrome type 8 (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Oro-facial digital syndrome type 8 (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 4
Oro-facial digital syndrome type 8 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Oro-facial digital syndrome type 8 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 5
Oro-facial digital syndrome type 8 (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Oro-facial digital syndrome type 8 (disorder) Finding site Face structure true Inferred relationship Some 2
Oro-facial digital syndrome type 8 (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Oro-facial digital syndrome type 8 (disorder) Associated morphology Dysplasia true Inferred relationship Some 5
Oro-facial digital syndrome type 8 (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Oro-facial digital syndrome type 8 (disorder) Is a X-linked recessive hereditary disease true Inferred relationship Some
Oro-facial digital syndrome type 8 (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Some 6
Oro-facial digital syndrome type 8 (disorder) Has interpretation Impaired true Inferred relationship Some 6
Oro-facial digital syndrome type 8 (disorder) Interprets Adaptation behavior (observable entity) true Inferred relationship Some 7
Oro-facial digital syndrome type 8 (disorder) Has interpretation Impaired true Inferred relationship Some 7

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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US English

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