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720565000: Bohring Opitz syndrome (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
3321255015 Bohring Opitz syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321256019 Bohring Opitz syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321257011 C-like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321258018 Opitz trigonocephaly-like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321259014 Bohring syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321260016 Syndrome with characteristics of intrauterine growth retardation, failure to thrive, facial dysmorphism, flexion deformities of the elbows and wrists, camptodactyly, ulnar deviation of the fingers, foot anomalies and severe developmental delay. Less than 20 patients have been described so far. Although the large majority of reported cases occurred sporadically, autosomal recessive inheritance has also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
10041401000172114 BOS - Bohring-Opitz syndrome fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
10041411000172112 syndrome de Bohring-Opitz fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
10041421000172119 syndrome 'C-like' fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
4167811000172116 Opitz trigonocefalie-'like' syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
4167821000172114 BOS nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
4167831000172112 C-achtig syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
4167841000172117 Oberklaid-Danks-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
4167851000172115 Bohring-Opitz-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
4167861000172118 'C-like' syndroom nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
4167871000172110 Opitz trigonocefalieachtig syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
4167881000172113 syndroom van Bohring-Opitz nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
4167891000172111 syndroom van Oberklaid-Danks nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Bohring Opitz syndrome (disorder) Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
Bohring Opitz syndrome (disorder) Is a Developmental delay true Inferred relationship Some
Bohring Opitz syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 2
Bohring Opitz syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Bohring Opitz syndrome (disorder) Finding site Limb structure true Inferred relationship Some 2
Bohring Opitz syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 3
Bohring Opitz syndrome (disorder) Occurrence Congenital false Inferred relationship Some 3
Bohring Opitz syndrome (disorder) Finding site Face structure false Inferred relationship Some 3
Bohring Opitz syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Bohring Opitz syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Bohring Opitz syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Bohring Opitz syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Bohring Opitz syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Bohring Opitz syndrome (disorder) Finding site Face structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Belgian subset for medical problems in patient health records

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