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716231009: Spondylocamptodactyly syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3305155014 Spondylocamptodactyly syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3305156010 Spondylocamptodactyly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3305157018 Rare syndrome with characteristics of camptodactyly, flattened cervical vertebral bodies and variable degrees of thoracic scoliosis. This syndrome has been described in five members from three generations of one family. Inheritance is thought to be autosomal dominant or autosomal recessive with pseudodominance. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
923701000172119 syndrome spondylo-camptodactylie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
975491000172117 spondylocamptodactyliesyndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spondylocamptodactyly syndrome (disorder) Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Spondylocamptodactyly syndrome (disorder) Is a Spondylodysplastic group true Inferred relationship Some
Spondylocamptodactyly syndrome (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Spondylocamptodactyly syndrome (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Spondylocamptodactyly syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 2
Spondylocamptodactyly syndrome (disorder) Occurrence Congenital false Inferred relationship Some 2
Spondylocamptodactyly syndrome (disorder) Finding site Bone structure false Inferred relationship Some 2
Spondylocamptodactyly syndrome (disorder) Finding site Bone structure true Inferred relationship Some 1
Spondylocamptodactyly syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Spondylocamptodactyly syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Spondylocamptodactyly syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 1
Spondylocamptodactyly syndrome (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Spondylocamptodactyly syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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