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880067009: Blount disease (disorder)


Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3994407018 Blount disease en Synonym Active Case sensitive SNOMED CT core
3994408011 Blount disease (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3994414016 Osteochondrosis deformans tibiae-familial infantile type en Synonym Active Case insensitive SNOMED CT core
3994420015 Osteochondrosis deformans tibiae en Synonym Active Case insensitive SNOMED CT core
4011884013 Infantile tibia vara en Synonym Active Case insensitive SNOMED CT core
4011885014 Tibia vara Blount en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Blount disease Finding site Bone structure of tibia true Inferred relationship Some 1
Blount disease Associated morphology Varus deformity true Inferred relationship Some 1
Blount disease Is a Varus deformity of tibia true Inferred relationship Some
Blount disease Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Blount disease Is a Autosomal hereditary disorder 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

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