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203522001: Osteolysis (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
312253017 Osteolysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
588634013 Osteolysis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1494969016 Osteolytic lesion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
941331000195117 osteolisi it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
77481000077110 ostéolyse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

53 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteolysis Is a Disorder of bone and articular cartilage false Inferred relationship Some
Osteolysis Finding site Cartilaginous tissue structure false Inferred relationship Some
Osteolysis Finding site Bone structure false Inferred relationship Some 1
Osteolysis Finding site Skeletal system structure false Inferred relationship Some
Osteolysis Is a Disorder of bone (disorder) false Inferred relationship Some
Osteolysis Associated morphology Lysis (morphologic abnormality) false Inferred relationship Some
Osteolysis Associated morphology Osteolysis false Inferred relationship Some 1
Osteolysis Is a Degenerative disorder false Inferred relationship Some
Osteolysis Finding site Bone structure true Inferred relationship Some 1
Osteolysis Associated morphology Osteolysis true Inferred relationship Some 1
Osteolysis Is a Degenerative disorder of bone true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Osteolytic lesion Is a False Osteolysis Inferred relationship Some
Gorham's disease Is a True Osteolysis Inferred relationship Some
Migratory osteolysis Is a False Osteolysis Inferred relationship Some
Migratory osteolysis Is a True Osteolysis Inferred relationship Some
Periprosthetic osteolysis Is a True Osteolysis Inferred relationship Some
An early-onset distal osteolysis characterized by severe resorption of the hands and feet and absence of the distal and middle phalanges. It has been described in a son and daughter born to consanguineous parents. Other manifestations include distal muscular hypertrophy, flexion contractures, short stature, mild intellectual deficit and characteristic facies (maxillary hypoplasia, exophthalmos, and a broad nasal tip). It is transmitted as an autosomal recessive trait. Is a True Osteolysis Inferred relationship Some
A rare systemic or rheumatologic disease characterized by peripheral osteolysis (especially carpal and tarsal bones), interphalangeal joint erosions, subcutaneous fibrocollagenous nodules, facial dysmorphism, and a wide range of associated manifestations. Is a True Osteolysis Inferred relationship Some
ostéomyélite chronique à cellules plasmatiques symétriques Is a False Osteolysis Inferred relationship Some
A rare primary bone dysplasia characterized by extensive epiphyseal, tarsal, spinal, and sometimes metacarpal and/or phalangeal stippling, severe generalized osteopenia, vertebral clefting, platyspondyly, bowing and shortening of the long bones, and variable periosteal cloaking. Laboratory analysis of lysosomal enzymes reveals normal activity. Histopathology shows numerous giant, multinucleated osteoclasts lining Howship lacunae, consistent with increased bone resorption. The condition manifests prenatally and is presumably lethal in the perinatal period. Is a True Osteolysis Inferred relationship Some
Talo-patello-scaphoid osteolysis is an extremely rare form of primary osteolysis, described in two sisters to date, characterized by bilateral osteolysis of the tali, scaphoids, and patellae (accompanied by periarticular swelling and pain) and short fourth metacarpals, in the absence of renal disease. Autosomal recessive inheritance has been suggested. Is a True Osteolysis Inferred relationship Some
Osteolysis following surgical procedure on skeletal system Is a True Osteolysis Inferred relationship Some
Osteolysis of right distal clavicle Is a False Osteolysis Inferred relationship Some
Osteolysis of left distal clavicle (disorder) Is a False Osteolysis Inferred relationship Some
A rare primary osteolysis disorder characterized by multiple small osteolytic areas and sclerosis in the phalanges of one or both hands associated with swelling and redness of the phalanges. Condition is benign, self-limited and may be associated with cold exposure. Is a True Osteolysis Inferred relationship Some
Nestor-Guillermo progeria syndrome is a rare, genetic, progeroid syndrome characterized by a prematurely aged appearance associated with severe osteolysis (notably on mandible, clavicles, ribs, distal phalanges, and long bones), osteoporosis, generalized lipoatrophy and absence of cardiovascular, atherosclerotic and metabolic complications, presenting a relatively long survival. Additional characteristics include growth retardation, joint stiffness (mainly of fingers, hands, knees, and elbows), wide cranial sutures, dysmorphic facial features (prominent eyes, convex nasal ridge, malocclusion, dental crowding, thin lip vermillion, microretrognathia) and persistent eyebrows, eyelashes and scalp hair. Is a True Osteolysis Inferred relationship Some
Idiopathic osteolyses Is a True Osteolysis Inferred relationship Some
Winchester syndrome Is a True Osteolysis Inferred relationship Some
Osteolysis of left foot Is a False Osteolysis Inferred relationship Some
Osteolysis of right foot Is a False Osteolysis Inferred relationship Some
Osteolysis due to and following traumatic injury (disorder) Is a True Osteolysis Inferred relationship Some
Secondary osteolysis (disorder) Is a True Osteolysis Inferred relationship Some
A rare genetic disease characterised by infantile or childhood onset of abnormal growth of hyalinised fibrous tissue, giving rise to multiple cutaneous nodules and/or pearly papules predominantly affecting the scalp, ears, neck, face, hands, and feet. Involvement of other organs results in gingival hyperplasia, osteolytic bone lesions, and joint contractures. Some patients exhibit visceral involvement with intractable diarrhoea, increased susceptibility to infections, and severe failure to thrive. Is a True Osteolysis Inferred relationship Some
Osteolysis of thoracic vertebra Is a True Osteolysis Inferred relationship Some
Osteolysis of tibia Is a True Osteolysis Inferred relationship Some
Osteolysis of humerus (disorder) Is a True Osteolysis Inferred relationship Some
Osteolysis of radius Is a True Osteolysis Inferred relationship Some
Osteolysis of femur (disorder) Is a True Osteolysis Inferred relationship Some
Osteolysis of acromial end of clavicle Is a True Osteolysis Inferred relationship Some
Osteolysis of foot Is a True Osteolysis Inferred relationship Some

This concept is not in any reference sets

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