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715440003: Laurin-Sandrow-syndroom (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3302639010 Mirror hands and feet co-occurrent with nasal defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302640012 Mirror hands and feet co-occurrent with nasal defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302641011 Laurin Sandrow syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3302642016 Sandrow syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6999731000146113 syndroom van Laurin-Sandrow nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7027641000146117 syndroom van Sandrow nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7904971000146113 gespiegelde handen en voeten gelijktijdig met neusdefect nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10669561000146116 Laurin-Sandrow-syndroom (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10669571000146110 Laurin-Sandrow-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3302643014 Complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis). 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
Mirror hands and feet co-occurrent with nasal defect (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Mirror hands and feet co-occurrent with nasal defect (disorder) Is a polysyndactyliesyndroom false Inferred relationship Some
Mirror hands and feet co-occurrent with nasal defect (disorder) Is a Dysostosis of bone of skull false Inferred relationship Some
Mirror hands and feet co-occurrent with nasal defect (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Mirror hands and feet co-occurrent with nasal defect (disorder) Is a Hereditary disorder of musculoskeletal system false Inferred relationship Some
Mirror hands and feet co-occurrent with nasal defect (disorder) Occurrence Congenital true Inferred relationship Some 2
Mirror hands and feet co-occurrent with nasal defect (disorder) Occurrence Congenital true Inferred relationship Some 3
Mirror hands and feet co-occurrent with nasal defect (disorder) Associated morphology congenitale afwijkende fusie false Inferred relationship Some 2
Mirror hands and feet co-occurrent with nasal defect (disorder) Finding site Digit structure true Inferred relationship Some 2
Mirror hands and feet co-occurrent with nasal defect (disorder) Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 3
Mirror hands and feet co-occurrent with nasal defect (disorder) Finding site Bone structure of cranium false Inferred relationship Some 3
Mirror hands and feet co-occurrent with nasal defect (disorder) Associated morphology Supernumerary structure false Inferred relationship Some 1
Mirror hands and feet co-occurrent with nasal defect (disorder) Occurrence Congenital true Inferred relationship Some 1
Mirror hands and feet co-occurrent with nasal defect (disorder) Finding site Digit structure true Inferred relationship Some 1
Mirror hands and feet co-occurrent with nasal defect (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Mirror hands and feet co-occurrent with nasal defect (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Mirror hands and feet co-occurrent with nasal defect (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Mirror hands and feet co-occurrent with nasal defect (disorder) Associated morphology Supernumerary structure true Inferred relationship Some 2
Mirror hands and feet co-occurrent with nasal defect (disorder) Associated morphology congenitale afwijkende fusie false Inferred relationship Some 1
Mirror hands and feet co-occurrent with nasal defect (disorder) Associated morphology Dysplasia false Inferred relationship Some 3
Mirror hands and feet co-occurrent with nasal defect (disorder) Is a Polysyndactyly (disorder) true Inferred relationship Some
Mirror hands and feet co-occurrent with nasal defect (disorder) Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Mirror hands and feet co-occurrent with nasal defect (disorder) Is a Congenital anomaly of nose true Inferred relationship Some
Mirror hands and feet co-occurrent with nasal defect (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Mirror hands and feet co-occurrent with nasal defect (disorder) Finding site Nasal structure true Inferred relationship Some 3
Mirror hands and feet co-occurrent with nasal defect (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Mirror hands and feet co-occurrent with nasal defect (disorder) Associated morphology Abnormally fused structure (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

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