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787407003: Muenke syndrome (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
3775317012 Muenke syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3775318019 Muenke syndrome (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
Muenke syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Muenke syndrome Is a Fibroblast growth factor receptor 3-related craniosynostosis true Inferred relationship Existential restriction modifier
Muenke syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Muenke syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Muenke syndrome Finding site Structure of coronal suture of skull true Inferred relationship Existential restriction modifier 1
Muenke syndrome Associated morphology Congenital premature fusion true Inferred relationship Existential restriction modifier 1
Muenke syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Muenke syndrome Is a Congenital anomaly of bone and joint false Inferred relationship Existential restriction modifier
Muenke syndrome Is a Congenital anomaly of skull false Inferred relationship Existential restriction modifier
Muenke syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Muenke 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

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