FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.8.2 | FHIR Version n/a User: [n/a]

49347007: Osteosclerosis (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteosclerosis
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Osteosclerosis
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteosclerosis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteosclerosis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteosclerosis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Osteosclerosis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Osteosclerosis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteosclerosis
\Disease\Chronic disease\Chronic disease of musculoskeletal system\Osteosclerosis
\Disease\Developmental disorder\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Osteosclerosis
\Disease\Developmental disorder\Developmental hereditary disorder\Osteosclerosis
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteosclerosis

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

1998431000005118 osteosklerose da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

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
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.	Is a	True	Osteosclerosis	Inferred relationship	Some
Piriform sclerosis of ilium	Is a	False	Osteosclerosis	Inferred relationship	Some
Chronic symmetric plasma cell osteomyelitis	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 (disorder)	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

This concept is not in any reference sets

Back to Start

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
1998431000005118	osteosklerose	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)