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719019000: WT-bloedsyndroom van extremiteit (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
3314688017 WT limb blood syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3314689013 WT limb blood syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6927031000146114 WT-bloedsyndroom van ledemaat nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7712071000146111 WT-bloedsyndroom van extremiteit nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7712081000146113 WT-bloedsyndroom van extremiteit (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3314690016 Syndrome is characterised by haematological anomalies (Fanconi anaemia, leukaemia and lymphoma) often appearing during childhood. Anomalies of the limbs and hands are also present: bifid or hypoplastic thumbs, cutaneous syndactyly and ulnar and radial defects. The syndrome has been described in several families. Transmission is autosomal dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3314691017 Syndrome is characterized by hematological anomalies (Fanconi anemia, leukemia and lymphoma) often appearing during childhood. Anomalies of the limbs and hands are also present: bifid or hypoplastic thumbs, cutaneous syndactyly and ulnar and radial defects. The syndrome has been described in several families. Transmission is autosomal dominant. 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
WT limb blood syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
WT limb blood syndrome (disorder) Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
WT limb blood syndrome (disorder) Is a Aplastic anaemia false Inferred relationship Some
WT limb blood syndrome (disorder) Is a Hereditary disorder of cellular element of blood (disorder) false Inferred relationship Some
WT limb blood syndrome (disorder) Has definitional manifestation Cytopenia false Inferred relationship Some
WT limb blood syndrome (disorder) Occurrence Congenital true Inferred relationship Some 4
WT limb blood syndrome (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
WT limb blood syndrome (disorder) Occurrence Congenital false Inferred relationship Some 3
WT limb blood syndrome (disorder) Associated morphology Aplasia true Inferred relationship Some 4
WT limb blood syndrome (disorder) Finding site Bone marrow structure true Inferred relationship Some 4
WT limb blood syndrome (disorder) Has interpretation Below reference range true Inferred relationship Some 2
WT limb blood syndrome (disorder) Has interpretation Below reference range true Inferred relationship Some 5
WT limb blood syndrome (disorder) Has interpretation Below reference range true Inferred relationship Some 3
WT limb blood syndrome (disorder) Interprets Red blood cell count true Inferred relationship Some 5
WT limb blood syndrome (disorder) Has interpretation Below reference range true Inferred relationship Some 1
WT limb blood syndrome (disorder) Interprets Platelet count true Inferred relationship Some 3
WT limb blood syndrome (disorder) Due to Decreased erythrocyte production true Inferred relationship Some 6
WT limb blood syndrome (disorder) Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 1
WT limb blood syndrome (disorder) Is a Inherited platelet disorder true Inferred relationship Some
WT limb blood syndrome (disorder) Is a Hereditary white blood cell disorder (disorder) true Inferred relationship Some
WT limb blood syndrome (disorder) Is a Constitutional aplastic anemia true Inferred relationship Some
WT limb blood syndrome (disorder) Interprets White blood cell count true Inferred relationship Some 2
WT limb blood syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
WT limb blood syndrome (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 8
WT limb blood syndrome (disorder) Has interpretation Abnormal false Inferred relationship Some 7
WT limb blood syndrome (disorder) Interprets Hemostatic function true Inferred relationship Some 7
WT limb blood syndrome (disorder) Has interpretation Abnormal true Inferred relationship Some 7
WT limb blood syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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