FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

782786001: X-linked calvarial hyperostosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3755757014 X-linked calvarial hyperostosis en Synonym Active Entire term case sensitive SNOMED CT core module
3755758016 X-linked calvarial hyperostosis (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked calvarial hyperostosis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
X-linked calvarial hyperostosis Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
X-linked calvarial hyperostosis Is a Dysplasia with decreased bone density true Inferred relationship Existential restriction modifier
X-linked calvarial hyperostosis Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
X-linked calvarial hyperostosis Finding site Bone structure true Inferred relationship Existential restriction modifier 1
X-linked calvarial hyperostosis Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
X-linked calvarial hyperostosis Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
X-linked calvarial hyperostosis Interprets Bone density scan true Inferred relationship Existential restriction modifier 2
X-linked calvarial hyperostosis Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
X-linked calvarial hyperostosis Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
X-linked calvarial hyperostosis Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start