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722117000: Osteosclerosis, developmental delay, craniosynostosis 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
5402833011 This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402834017 This newly described syndrome is characterised by osteosclerosis, developmental delay and craniosynostosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330762013 Osteosclerosis, developmental delay, craniosynostosis syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330765010 Osteosclerosis, developmental delay, craniosynostosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6455681000241113 syndrome d'ostéosclérose, retard de développement et craniosténose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6455691000241110 syndrome d'ostéosclérose, retard de développement et craniosynostose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3440261001000114 Osteosklerose-Entwicklungsverzögerung-Kraniosynostose-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
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Is a Autosomal dominant hereditary disorder (disorder) true Inferred relationship Some
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Is a Osteosclerosis false Inferred relationship Some
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Is a Congenital connective tissue disorder false Inferred relationship Some
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Is a Connective tissue hereditary disorder false Inferred relationship Some
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Associated morphology Bony sclerosis true Inferred relationship Some 2
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Occurrence Congenital true Inferred relationship Some 2
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Finding site Bone structure true Inferred relationship Some 2
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Occurrence Congenital false Inferred relationship Some 3
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Associated morphology anomalie du développement false Inferred relationship Some 2
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Finding site Face structure false Inferred relationship Some 2
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Associated morphology Bony sclerosis false Inferred relationship Some 3
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Finding site Bone structure false Inferred relationship Some 3
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Occurrence Congenital true Inferred relationship Some 1
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Is a Congenital anomaly of skeletal bone true Inferred relationship Some
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Finding site Face structure true Inferred relationship Some 1
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Is a Developmental hereditary disorder 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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