FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

19092004: Holt-Oram syndrome (disorder)


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
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
32179011 Holt-Oram syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
32180014 Cardiac-limb syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
32181013 Atrio-digital syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
746856019 Holt-Oram syndrome (disorder) en Fully specified name Active Only initial character case insensitive (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 Only initial character case insensitive (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 Only initial character 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
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
3432931001000114 Holt-Oram-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
979781000172110 dysplasie atrio-digitale type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1006391000172117 syndrome de Holt-Oram fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
979781000172110 dysplasie atrio-digitale type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1006391000172117 syndrome de Holt-Oram fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3432931001000114 Holt-Oram-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


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 Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Is a Congenital anomaly of limb false Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Finding site Musculoskeletal structure of limb (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Is a Structural disorder of heart false Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Holt-Oram syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Holt-Oram syndrome Finding site Cardiac structure false Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Finding site Heart structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Holt-Oram syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Holt-Oram syndrome Finding site Cardiac structure false Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Associated morphology Mechanical abnormality (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Holt-Oram syndrome Is a Congenital heart disease (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Finding site Heart structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Holt-Oram syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Holt-Oram syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Holt-Oram syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Holt-Oram syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Holt-Oram syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Holt-Oram syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Holt-Oram syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Holt-Oram syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 4
Holt-Oram syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Holt-Oram syndrome Is a Congenital heart disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Finding site Heart structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Holt-Oram syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Holt-Oram syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Is a Congenital anomaly of upper limb true Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Is a Dysostosis true Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Is a Finding of bone of upper limb true Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Is a A disorder in which there is abnormal electrical activity in the heart. true Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Holt-Oram syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Holt-Oram syndrome Finding site Bone structure of upper limb (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Holt-Oram syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Holt-Oram syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Holt-Oram syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Holt-Oram syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Is a Congenital dysplasia of limb (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Holt-Oram syndrome Finding site Cardiac conducting system structure true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start