FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

19092004: hart-handsyndroom type 1 (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
32179011 Holt-Oram syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
746856019 Holt-Oram syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2923360019 Holt Oram syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3323026012 Heart-hand syndrome type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3323027015 Atriodigital dysplasia type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5059701000146116 HOS nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5059711000146119 hart-handsyndroom type 1 (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5059721000146112 hart-handsyndroom type 1 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5059731000146114 Holt-Oram-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5059741000146118 atriodigitale dysplasie type 1 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12664761000146118 holt-oramsyndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3323037013 Holt-Oram syndrome is the most common form of heart-hand syndrome with characteristics of skeletal abnormalities of the upper limbs and mild-to-severe congenital cardiac defects. The clinical picture of covers a wide spectrum of upper extremity defects, always including the radial ray, and cardiac defects. Caused by a mutation in the TBX5 gene located on the long arm of chromosome 12 (12q24.1). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
13080391000146118 Erfelijke en aangeboren aandoening gekenmerkt door afwijkingen aan de armen en/of handen in combinatie met hartafwijkingen. nl Definition Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Holt-Oram syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Holt-Oram syndrome Is a Congenital anomaly of limb false Inferred relationship Some
Holt-Oram syndrome Finding site Musculoskeletal structure of limb false Inferred relationship Some
Holt-Oram syndrome Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some
Holt-Oram syndrome Occurrence Congenital false Inferred relationship Some
Holt-Oram syndrome Is a Structural disorder of heart false Inferred relationship Some
Holt-Oram syndrome Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 1
Holt-Oram syndrome Finding site Limb structure false Inferred relationship Some 1
Holt-Oram syndrome Finding site Cardiac structure false Inferred relationship Some
Holt-Oram syndrome Finding site Heart structure false Inferred relationship Some 2
Holt-Oram syndrome Associated morphology Congenital malformation false Inferred relationship Some 1
Holt-Oram syndrome Finding site Cardiac structure false Inferred relationship Some
Holt-Oram syndrome Associated morphology Mechanical abnormality false Inferred relationship Some 2
Holt-Oram syndrome Is a Congenital heart disease false Inferred relationship Some
Holt-Oram syndrome Finding site Heart structure true Inferred relationship Some 2
Holt-Oram syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some 2
Holt-Oram syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Holt-Oram syndrome Finding site Limb structure false Inferred relationship Some 1
Holt-Oram syndrome Associated morphology Congenital malformation false Inferred relationship Some 1
Holt-Oram syndrome Occurrence Congenital false Inferred relationship Some 3
Holt-Oram syndrome Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
Holt-Oram syndrome Occurrence Congenital false Inferred relationship Some 4
Holt-Oram syndrome Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 4
Holt-Oram syndrome Finding site Limb structure false Inferred relationship Some 4
Holt-Oram syndrome Is a Congenital heart disease true Inferred relationship Some
Holt-Oram syndrome Finding site Heart structure false Inferred relationship Some 3
Holt-Oram syndrome Occurrence Congenital true Inferred relationship Some 2
Holt-Oram syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Holt-Oram syndrome Is a Congenital anomaly of upper limb true Inferred relationship Some
Holt-Oram syndrome Is a Dysostosis true Inferred relationship Some
Holt-Oram syndrome Is a Finding of bone of upper limb true Inferred relationship Some
Holt-Oram syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Some
Holt-Oram syndrome Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Holt-Oram syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Holt-Oram syndrome Is a Cardiac arrhythmia (disorder) true Inferred relationship Some
Holt-Oram syndrome Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 1
Holt-Oram syndrome Occurrence Congenital true Inferred relationship Some 1
Holt-Oram syndrome Finding site Bone structure of upper limb (body structure) true Inferred relationship Some 1
Holt-Oram syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Holt-Oram syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Holt-Oram syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Holt-Oram syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Holt-Oram syndrome Is a Congenital dysplasia of limb (disorder) true Inferred relationship Some
Holt-Oram syndrome Finding site Cardiac conducting system structure true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start