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763684005: Craniosynostosis Herrmann Opitz type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3643279010 Craniosynostosis Herrmann Opitz type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3643280013 Craniosynostosis Herrmann Opitz type en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Craniosynostosis Herrmann Opitz type Is a Craniosynostosis syndrome true Inferred relationship Existential restriction modifier
Craniosynostosis Herrmann Opitz type Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier
Craniosynostosis Herrmann Opitz type Associated morphology Congenital premature fusion true Inferred relationship Existential restriction modifier 1
Craniosynostosis Herrmann Opitz type Finding site Joint structure of suture of skull true Inferred relationship Existential restriction modifier 1
Craniosynostosis Herrmann Opitz type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Craniosynostosis Herrmann Opitz type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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