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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
82200018 Osteosclerosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
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 Existential restriction modifier (core metadata concept)
Osteosclerosis Associated morphology Bony sclerosis false Inferred relationship Existential restriction modifier (core metadata concept)
Osteosclerosis Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept)
Osteosclerosis Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Osteosclerosis Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteosclerosis Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteosclerosis Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Osteosclerosis Associated morphology Bony sclerosis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteosclerosis Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier (core metadata concept)
Osteosclerosis Is a Chronic disease of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Osteosclerosis Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteosclerosis Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2
Osteosclerosis Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Osteosclerosis - Stanescu type Is a False Osteosclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Axial osteosclerosis Is a True Osteosclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Piriform sclerosis of ilium Is a False Osteosclerosis Inferred relationship Existential restriction modifier (core metadata concept)
ostéomyélite chronique à cellules plasmatiques symétriques Is a False Osteosclerosis Inferred relationship Existential restriction modifier (core metadata concept)
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis. Is a False Osteosclerosis Inferred relationship Existential restriction modifier (core metadata concept)
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 Existential restriction modifier (core metadata concept)
Melorheostosis Is a False Osteosclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Short stature disorder due to osteosclerosis (disorder) Due to True Osteosclerosis Inferred relationship Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept)
Osteosclerotic metaphyseal dysplasia (disorder) Is a True Osteosclerosis Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant osteopetrosis type 1 (disorder) Is a True Osteosclerosis Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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