FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

732250002: Craniosynostosis fibular aplasia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3464760016 Craniosynostosis fibular aplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3464761017 Craniosynostosis fibular aplasia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3464762012 Lowry syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Craniosynostosis fibular aplasia syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier
Craniosynostosis fibular aplasia syndrome Is a Congenital anomaly of skull false Inferred relationship Existential restriction modifier
Craniosynostosis fibular aplasia syndrome Is a Craniosynostosis syndrome true Inferred relationship Existential restriction modifier
Craniosynostosis fibular aplasia syndrome Is a Congenital absence of fibula false Inferred relationship Existential restriction modifier
Craniosynostosis fibular aplasia syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Craniosynostosis fibular aplasia syndrome Is a Congenital anomaly of bone and joint true Inferred relationship Existential restriction modifier
Craniosynostosis fibular aplasia syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Craniosynostosis fibular aplasia syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Craniosynostosis fibular aplasia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Craniosynostosis fibular aplasia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Craniosynostosis fibular aplasia syndrome Associated morphology Congenital premature fusion false Inferred relationship Existential restriction modifier 2
Craniosynostosis fibular aplasia syndrome Finding site Structure of coronal suture of skull false Inferred relationship Existential restriction modifier 2
Craniosynostosis fibular aplasia syndrome Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 3
Craniosynostosis fibular aplasia syndrome Finding site Bone structure of fibula false Inferred relationship Existential restriction modifier 3
Craniosynostosis fibular aplasia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Craniosynostosis fibular aplasia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Craniosynostosis fibular aplasia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Craniosynostosis fibular aplasia syndrome Finding site Structure of coronal suture of skull true Inferred relationship Existential restriction modifier 1
Craniosynostosis fibular aplasia syndrome Associated morphology Congenital premature fusion true Inferred relationship Existential restriction modifier 1
Craniosynostosis fibular aplasia syndrome Finding site Entire fibula true Inferred relationship Existential restriction modifier 2
Craniosynostosis fibular aplasia syndrome Associated morphology Agenesis true Inferred relationship Existential restriction modifier 2
Craniosynostosis fibular aplasia syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Craniosynostosis fibular aplasia syndrome Is a Agenesis of fibula true Inferred relationship Existential restriction modifier
Craniosynostosis fibular aplasia syndrome Is a Finding of head region 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