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774150004: Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3728147016 Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3728148014 Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3728149018 A rare genetic neural tube defect malformation syndrome with characteristics of sacral agenesis and abnormal vertebral body ossification with normal vertebral arches associated with notochord canal persistence on ultrasonography. Additional findings include bilateral clubfoot, oligohydramnios, and single umbilical artery and in some cases increased nuchal translucency. There is evidence the disease can be caused by homozygous mutation in the T gene on chromosome 6q27. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3728147016 Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3728148014 Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3728149018 A rare genetic neural tube defect malformation syndrome with characteristics of sacral agenesis and abnormal vertebral body ossification with normal vertebral arches associated with notochord canal persistence on ultrasonography. Additional findings include bilateral clubfoot, oligohydramnios, and single umbilical artery and in some cases increased nuchal translucency. There is evidence the disease can be caused by homozygous mutation in the T gene on chromosome 6q27. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3430041001000116 Sakrale Agenesie-abnormale Verknöcherung der Wirbelkörper-persistierender notochordaler Kanal-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
869861000172110 syndrome d'agénésie sacrée-ossification anormale des corps vertébraux-persistance de la notochorde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
869861000172110 syndrome d'agénésie sacrée-ossification anormale des corps vertébraux-persistance de la notochorde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3430041001000116 Sakrale Agenesie-abnormale Verknöcherung der Wirbelkörper-persistierender notochordaler Kanal-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
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Finding site Spinal cord structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Finding site Lumbosacral region of spine structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Is a Sacral agenesis true Inferred relationship Existential restriction modifier (core metadata concept)
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Finding site Neural tube structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Is a Neural tube defect true Inferred relationship Existential restriction modifier (core metadata concept)
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Associated morphology Agenesis (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Finding site Entire sacral vertebral column false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Finding site Structure of sacral vertebral column region (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Is a Congenital anomaly of spinal cord true Inferred relationship Existential restriction modifier (core metadata concept)
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) Finding site Entire sacral vertebral column region true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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