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725166005: Autosomal recessive omodysplasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3439991011 Autosomal recessive omodysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3439992016 Autosomal recessive omodysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3439993014 Micromelic dysplasia, dislocation of radius syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3439994015 Omodysplasia 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
903351000172110 syndrome de dysplasie micromélique, dysplasie du radius fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
945131000172110 omodysplasie autosomique récessive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3451081001000117 Omodysplasie, autosomal-rezessive Form 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
Autosomal recessive omodysplasia (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Autosomal recessive omodysplasia (disorder) Is a Omodysplasia is a rare skeletal dysplasia characterized by severe limb shortening and facial dysmorphism. Two types of omodysplasia have been described: an autosomal recessive or generalized form (also referred to as micromelic dysplasia with dislocation of radius) marked by severe micromelic dwarfism with predominantly rhizomelic shortening of both the upper and lower limbs, and an autosomal dominant form in which stature is normal and shortening is limited to the upper limbs. true Inferred relationship Some
Autosomal recessive omodysplasia (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 1
Autosomal recessive omodysplasia (disorder) Occurrence Congenital true Inferred relationship Some 1
Autosomal recessive omodysplasia (disorder) Finding site Bone structure false Inferred relationship Some 1
Autosomal recessive omodysplasia (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal recessive omodysplasia (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Autosomal recessive omodysplasia (disorder) Interprets Limb length true Inferred relationship Some 2
Autosomal recessive omodysplasia (disorder) Has interpretation Below reference range true Inferred relationship Some 2
Autosomal recessive omodysplasia (disorder) Finding site Bone structure of limb true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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