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254125009: Osteomesopyknosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
378292018 Axial osteosclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644973019 Axial osteosclerosis (disorder) en Fully specified name Inactive Entire term case insensitive (core metadata concept) SNOMED CT core
3786956012 Osteomesopycnosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5449354010 Osteomesopyknosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5449355011 Osteomesopyknosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3786957015 A very rare benign bone disorder with characteristics of bone dysplasia manifested by patchy sclerosis of the axial skeleton and increased bone mineral content. The disease may be underdiagnosed due to confusion with autosomal dominant osteopetrosis. The condition is usually found incidentally on radiological examination and is very mild, sometimes accompanied by pain. Increased density of the vertebral plates, pelvis and occasionally of the upper femur have been reported, as well as kyphoscoliosis and femoral cysts. en Definition Inactive Entire term case sensitive (core metadata concept) SNOMED CT core
5449356012 Osteomesopyknosis is a very rare benign bone disorder characterized by bone dysplasia manifested by patchy sclerosis of the axial skeleton and increased bone mineral content. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5449357015 Osteomesopyknosis is a very rare benign bone disorder characterised by bone dysplasia manifested by patchy sclerosis of the axial skeleton and increased bone mineral content. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteomesopyknosis (disorder) Is a Osteosclerosis true Inferred relationship Some
Osteomesopyknosis (disorder) Is a Dysplasia with increased bone density (disorder) true Inferred relationship Some
Osteomesopyknosis (disorder) Occurrence Congenital false Inferred relationship Some
Osteomesopyknosis (disorder) Finding site Skeletal system structure false Inferred relationship Some 1
Osteomesopyknosis (disorder) Finding site Bone structure of spine false Inferred relationship Some 1
Osteomesopyknosis (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Osteomesopyknosis (disorder) Associated morphology Bony sclerosis false Inferred relationship Some
Osteomesopyknosis (disorder) Is a Disorder of trunk (disorder) false Inferred relationship Some
Osteomesopyknosis (disorder) Is a Disorder of spine false Inferred relationship Some
Osteomesopyknosis (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 1
Osteomesopyknosis (disorder) Is a Congenital anomaly of spine false Inferred relationship Some
Osteomesopyknosis (disorder) Is a Finding of vertebra false Inferred relationship Some
Osteomesopyknosis (disorder) Finding site Bone structure of spine false Inferred relationship Some 1
Osteomesopyknosis (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 1
Osteomesopyknosis (disorder) Is a Disorder of vertebral column (disorder) false Inferred relationship Some
Osteomesopyknosis (disorder) Occurrence Congenital false Inferred relationship Some 2
Osteomesopyknosis (disorder) Associated morphology Dysplasia false Inferred relationship Some 2
Osteomesopyknosis (disorder) Finding site Bone structure false Inferred relationship Some 2
Osteomesopyknosis (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 2
Osteomesopyknosis (disorder) Occurrence Congenital true Inferred relationship Some 4
Osteomesopyknosis (disorder) Finding site Bone structure true Inferred relationship Some 4
Osteomesopyknosis (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Osteomesopyknosis (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
Osteomesopyknosis (disorder) Interprets Bone density scan true Inferred relationship Some 3
Osteomesopyknosis (disorder) Has interpretation Above reference range true Inferred relationship Some 3
Osteomesopyknosis (disorder) Finding site Skeletal system structure false Inferred relationship Some 2
Osteomesopyknosis (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Osteomesopyknosis (disorder) Associated morphology Bony sclerosis true Inferred relationship Some 4
Osteomesopyknosis (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 5
Osteomesopyknosis (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Osteomesopyknosis (disorder) Finding site Bone structure true Inferred relationship Some 1
Osteomesopyknosis (disorder) Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Osteomesopycnosis Is a False Osteomesopyknosis (disorder) Inferred relationship Some

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

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