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

254114000: Singleton-Merten syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
378275010 Singleton-Merten syndrome en Synonym Active Case sensitive SNOMED CT core
644960018 Singleton-Merten syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Singleton-Merten syndrome Occurrence Congenital true Inferred relationship Some 1
Singleton-Merten syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Singleton-Merten syndrome Interprets Bone density scan true Inferred relationship Some 2
Singleton-Merten syndrome Has interpretation Below reference range true Inferred relationship Some 2
Singleton-Merten syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 1
Singleton-Merten syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 1
Singleton-Merten syndrome Finding site Bone structure false Inferred relationship Some 1
Singleton-Merten syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Singleton-Merten syndrome Finding site Skeletal system structure false Inferred relationship Some 1
Singleton-Merten syndrome Occurrence Congenital false Inferred relationship Some 2
Singleton-Merten syndrome Finding site Bone structure false Inferred relationship Some 2
Singleton-Merten syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 2
Singleton-Merten syndrome Occurrence Congenital false Inferred relationship Some
Singleton-Merten syndrome Finding site Bone structure true Inferred relationship Some 1
Singleton-Merten syndrome Is a Dysplasia with decreased bone density true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Back to Start