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88650009: Both upper extremities (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
146985017 Both upper extremities en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
831378018 Both upper extremities (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2845911000005111 Begge overekstremiteter da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Both upper extremities Is a Entire upper limb false Inferred relationship Some
Both upper extremities del af Entire upper body false Additional relationship Some
Both upper extremities Laterality Right and left (qualifier value) false Inferred relationship Some
Both upper extremities Is a Upper extremity, including shoulder, arm, forearm, wrist, and hand false Inferred relationship Some
Both upper extremities Is a Structure of left upper limb (body structure) false Inferred relationship Some
Both upper extremities Is a Structure of right upper limb (body structure) false Inferred relationship Some
Both upper extremities Is a Group of anatomical entities (body structure) false Inferred relationship Some
Both upper extremities Is a Structure of bilateral paired structures (body structure) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Achondrogenesis, type IB Finding site False Both upper extremities Inferred relationship Some
Achondrogenesis (disorder) Finding site False Both upper extremities Inferred relationship Some
Achondrogenesis, type IA Finding site False Both upper extremities Inferred relationship Some
A rare skeletal dysplasia with characteristics of peculiar facial anomalies, Pierre Robin sequence, cleft palate, shortening and bowing of long bones. Sexual ambiguity or female external genitalia is possible individuals with a male karyotype. The disorder is autosomal dominant; however, most cases are due to heterozygous de novo mutations in the SOX9 gene (localized to 17q24). In rare individuals the disorder is caused by chromosomal recombination (deletion or translocation) involving the region 17q24. Finding site False Both upper extremities Inferred relationship Some
A short-rib dysplasia with characteristics of narrow thorax, short limbs and radiological skeletal abnormalities including "trident" aspect of the acetabula and metaphyseal changes. In rare cases, postaxial polydactyly may also be present. The narrow thorax may cause neonatal respiratory failure, and may be associated with persistent respiratory manifestations. The growth rate is variable but may be almost normal. Intellectual development is normal. The molecular basis of the syndrome has been partially elucidated indicating involvement of the IFT80 (3q25.33), DYNC2H1 (11q22.3), WDR19 (4p14) and TTC21B (2q24.3) genes, each encoding an intraflagellar transport protein. The syndrome is transmitted as an autosomal recessive trait. Finding site False Both upper extremities Inferred relationship Some
Achondroplasia Finding site False Both upper extremities Inferred relationship Some
Achondrogenesis, type II Finding site False Both upper extremities Inferred relationship Some
Both hands Is a False Both upper extremities Inferred relationship Some
Both upper arms Is a False Both upper extremities Inferred relationship Some
Both forearms Is a False Both upper extremities Inferred relationship Some

This concept is not in any reference sets

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