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719471002: Cleidorhizomelic 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
3316466014 Cleidorhizomelic syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3316467017 Cleidorhizomelic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3316468010 Rhizomelic shortness with clavicular defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3316469019 Wallis Zieff Goldblatt syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402130011 Cleidorhizomelic syndrome is a rhizo-mesomelic dysplasia characterized by rhizomelic short stature/dwarfism in combination with lateral clavicular defects. Additional manifestations include brachydactyly with bilateral clinodactyly and hypoplastic middle phalanx of the fifth digit. X-ray demonstrated an apparent Y-shaped or bifid distal clavicle. Cleidorhizomelic syndrome has been reported in one family (mother and son) and is suspected to be transmitted in an autosomal dominant manner. There have been no further descriptions in the literature since 1988. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402131010 Cleidorhizomelic syndrome is a rhizo-mesomelic dysplasia characterised by rhizomelic short stature/dwarfism in combination with lateral clavicular defects. Additional manifestations include brachydactyly with bilateral clinodactyly and hypoplastic middle phalanx of the fifth digit. X-ray demonstrated an apparent Y-shaped or bifid distal clavicle. Cleidorhizomelic syndrome has been reported in one family (mother and son) and is suspected to be transmitted in an autosomal dominant manner. There have been no further descriptions in the literature since 1988. 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
Cleidorhizomelic syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Cleidorhizomelic syndrome (disorder) Is a Mesomelic dysplasia false Inferred relationship Some
Cleidorhizomelic syndrome (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Cleidorhizomelic syndrome (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Cleidorhizomelic syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 2
Cleidorhizomelic syndrome (disorder) Occurrence Congenital false Inferred relationship Some 2
Cleidorhizomelic syndrome (disorder) Finding site Bone structure false Inferred relationship Some 2
Cleidorhizomelic syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Cleidorhizomelic syndrome (disorder) Finding site Bone structure false Inferred relationship Some 1
Cleidorhizomelic syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 1
Cleidorhizomelic syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Cleidorhizomelic syndrome (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Cleidorhizomelic syndrome (disorder) Is a Congenital anomaly of skeletal bone false Inferred relationship Some
Cleidorhizomelic syndrome (disorder) Clinical course Progressive (qualifier value) false Inferred relationship Some 2
Cleidorhizomelic syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Cleidorhizomelic syndrome (disorder) Interprets Height / growth measure false Inferred relationship Some 3
Cleidorhizomelic syndrome (disorder) Interprets Limb length true Inferred relationship Some 2
Cleidorhizomelic syndrome (disorder) Has interpretation Below reference range true Inferred relationship Some 2
Cleidorhizomelic syndrome (disorder) Finding site Bone structure of extremity true Inferred relationship Some 1
Cleidorhizomelic syndrome (disorder) Is a Rhizomelic dysplasia (disorder) true Inferred relationship Some
Cleidorhizomelic syndrome (disorder) Is a Short stature disorder true Inferred relationship Some
Cleidorhizomelic syndrome (disorder) Is a Finding of clavicle structure true Inferred relationship Some
Cleidorhizomelic syndrome (disorder) Is a Congenital anomaly of bone of shoulder girdle (disorder) true Inferred relationship Some
Cleidorhizomelic syndrome (disorder) Interprets Body height measure (observable entity) true Inferred relationship Some 4
Cleidorhizomelic syndrome (disorder) Has interpretation Below reference range true Inferred relationship Some 4
Cleidorhizomelic syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Cleidorhizomelic syndrome (disorder) Finding site Bone structure of clavicle true Inferred relationship Some 3
Cleidorhizomelic syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Cleidorhizomelic syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Cleidorhizomelic syndrome (disorder) Is a Congenital anomaly of body wall true Inferred relationship Some
Cleidorhizomelic syndrome (disorder) Is a Congenital anomaly of thorax true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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