FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

49347007: Osteosclerosis (disorder)

Status: current, 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
82200018 Osteosclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
787015011 Osteosclerosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4551031000241115 ostéosclérose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteosclerosis Is a Disorder of bone (disorder) false Inferred relationship Some
Osteosclerosis Associated morphology Bony sclerosis false Inferred relationship Some
Osteosclerosis Finding site Bone structure false Inferred relationship Some
Osteosclerosis Finding site Skeletal system structure false Inferred relationship Some
Osteosclerosis Occurrence Congenital true Inferred relationship Some 1
Osteosclerosis Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Osteosclerosis Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Osteosclerosis Associated morphology Bony sclerosis true Inferred relationship Some 1
Osteosclerosis Is a Congenital anomaly of skeletal bone true Inferred relationship Some
Osteosclerosis Is a Chronic disease of musculoskeletal system true Inferred relationship Some
Osteosclerosis Finding site Bone structure true Inferred relationship Some 1
Osteosclerosis Clinical course Progressive true Inferred relationship Some 2
Osteosclerosis Is a Developmental hereditary disorder true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Osteosclerosis - Stanescu type Is a False Osteosclerosis Inferred relationship Some
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. Is a True Osteosclerosis Inferred relationship Some
sclérose piriforme de l'ilium Is a False Osteosclerosis Inferred relationship Some
ostéomyélite chronique à cellules plasmatiques symétriques Is a False Osteosclerosis Inferred relationship Some
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Is a False Osteosclerosis Inferred relationship Some
Dentin dysplasia-sclerotic bones syndrome is a rare, genetic odontologic disease characterized by the clinical, radiographic, and histologic features of dentine dysplasia and osteosclerosis of all long bones, with heavy cortical bone and narrowed or occluded marrow spaces. There have been no further descriptions in the literature since 1977. Is a True Osteosclerosis Inferred relationship Some
Melorheostosis Is a False Osteosclerosis Inferred relationship Some
Short stature disorder due to osteosclerosis (disorder) Due to True Osteosclerosis Inferred relationship Some 2
A rare primary bone dysplasia with increased bone density characterized by slowly progressive endosteal hyperostosis and osteosclerosis exclusively of the skull base and the calvaria, resulting in entrapment and dysfunction of cranial nerves I, II, V, VII, and VIII. First symptoms often appear during the second decade of life and include disturbances in smell, vision, facial sensation and expression, hearing, and balance, as well as headaches due to increased ocular and intracranial pressure. After the fourth decade, radiological progression is minimal, although decreased intracranial volume can lead to death in severe cases. Is a True Osteosclerosis Inferred relationship Some
A rare primary bone dysplasia characterized by osteosclerosis localized predominantly to the metaphyses and epiphyseal margins of the appendicular bones and metaphyseal equivalents of the axial bones, as well as the vertebral endplates, costal ends, and margins of the flat bones. The skull is usually unaffected. The condition is associated with developmental delay and hypotonia. Seizures and spastic paraplegia have also been reported. Serum alkaline phosphatase and urinary pyridinoline and deoxypyridinoline levels may be elevated. Is a True Osteosclerosis Inferred relationship Some
A rare sclerosing bone disorder characterized by skeletal densification that predominantly involves the cranial vault. Is a True Osteosclerosis Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

GB English

US English

Back to Start