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30425001: Osteolysis (morphologic abnormality)

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
50927011 Osteolysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
50928018 Osteolytic lesion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
761428011 Osteolysis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteolysis Is a Lysis false Inferred relationship Some
Osteolysis Is a Lysis (morphologic abnormality) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Vinyl chloride disease Associated morphology False Osteolysis Inferred relationship Some 1
Gorham's disease Associated morphology False Osteolysis Inferred relationship Some 1
Migratory osteolysis Associated morphology False Osteolysis Inferred relationship Some 1
Occupational acroosteolysis Associated morphology False Osteolysis Inferred relationship Some 1
Osteolysis Associated morphology False Osteolysis Inferred relationship Some 1
Osteolysis Associated morphology True Osteolysis Inferred relationship Some 1
Gorham's disease Associated morphology True Osteolysis Inferred relationship Some 1
Migratory osteolysis Associated morphology True Osteolysis Inferred relationship Some 1
Periprosthetic osteolysis Associated morphology False Osteolysis Inferred relationship Some 1
Periprosthetic osteolysis Associated morphology True Osteolysis Inferred relationship Some 1
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. Associated morphology False Osteolysis Inferred relationship Some 3
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. Associated morphology False Osteolysis Inferred relationship Some 5
ostéomyélite chronique à cellules plasmatiques symétriques Associated morphology False Osteolysis Inferred relationship Some 5
A rare genetic disease characterized by infantile onset of recurrent skin ulcerations, arthralgias, fever, peri-articular fistulous osteolysis, oligodontia, nail dystrophy, and keratitis. The disease takes a self-limiting course in childhood but results in severe cicatrization, chronic arthroses, pseudoacromegalic appearance of hands and feet, secondary scoliosis, and visual impairment. There have been no further descriptions in the literature since 1983. Associated morphology False Osteolysis Inferred relationship Some 5
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. Associated morphology True Osteolysis Inferred relationship Some 1
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. Associated morphology False Osteolysis Inferred relationship Some 2
Osteolysis following surgical procedure on skeletal system Associated morphology True Osteolysis Inferred relationship Some 2
Osteolysis of right distal clavicle Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of left distal clavicle (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
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. Associated morphology True Osteolysis Inferred relationship Some 1
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. Associated morphology True Osteolysis Inferred relationship Some 1
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. Associated morphology True Osteolysis Inferred relationship Some 1
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. Associated morphology True Osteolysis Inferred relationship Some 1
A rare genetic disease characterized by infantile onset of recurrent skin ulcerations, arthralgias, fever, peri-articular fistulous osteolysis, oligodontia, nail dystrophy, and keratitis. The disease takes a self-limiting course in childhood but results in severe cicatrization, chronic arthroses, pseudoacromegalic appearance of hands and feet, secondary scoliosis, and visual impairment. There have been no further descriptions in the literature since 1983. Associated morphology True Osteolysis Inferred relationship Some 1
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. Associated morphology True Osteolysis Inferred relationship Some 2
Carpal-tarsal osteolysis with nephropathy (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Winchester syndrome Associated morphology False Osteolysis Inferred relationship Some 2
Torg type osteolysis Associated morphology True Osteolysis Inferred relationship Some 1
Familial expansile osteolysis Associated morphology True Osteolysis Inferred relationship Some 1
A very rare syndrome characterized by progressive loss of bone, usually the carpal and tarsal bones, resulting in deformity and disability, as well as chronic renal failure in many cases. The bone and renal disorders are sometimes associated with intellectual deficit and facial abnormalities. Associated morphology True Osteolysis Inferred relationship Some 1
Idiopathic multicentric osteolysis Associated morphology True Osteolysis Inferred relationship Some 1
Idiopathic osteolyses Associated morphology True Osteolysis Inferred relationship Some 1
Whyte Hemingway carpal tarsal phalangeal osteolyses (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Winchester syndrome Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of left foot Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of right foot Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis due to and following traumatic injury (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Secondary osteolysis (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Psoriatic arthritis mutilans Associated morphology True Osteolysis Inferred relationship Some 2
Arthritis mutilans Associated morphology True Osteolysis Inferred relationship Some 2
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. Associated morphology True Osteolysis Inferred relationship Some 1
A rare hyaline fibromatosis syndrome with characteristics of papulo-nodular skin lesions (especially around the head and neck), soft tissue masses, gingival hypertrophy, joint contractures and osteolytic bone lesions in variable degrees. Joint contractures may cripple patients and delay normal motor development if occurring in infancy. Severe gingival hyperplasia can interfere with eating and delay dentition. Histopathology analysis of involved tissues reveals cords of spindle-shaped cells embedded in an amorphous, hyaline material. Associated morphology True Osteolysis Inferred relationship Some 3
Infantile systemic hyalinosis (ISH) is a very rare disorder belonging to the heterogeneous group of genetic fibromatoses and is characterized by progressive joint contractures, skin abnormalities, severe chronic pain and widespread deposition of hyaline material in many tissues such as the skin, skeletal muscle, cardiac muscle, gastrointestinal tract, lymph nodes, spleen, thyroid, and adrenal glands. Associated morphology True Osteolysis Inferred relationship Some 2
Osteolysis of bone adjacent to left hip joint prosthesis Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of bone adjacent to right hip joint prosthesis Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of bone adjacent to left knee joint prosthesis (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of bone adjacent to hip joint prosthesis Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of bone adjacent to right knee joint prosthesis (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of bone adjacent to knee joint prosthesis (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Lytic lesion of bone on plain X-ray (finding) Associated morphology True Osteolysis Inferred relationship Some 2
Osteolysis of left humerus (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of right humerus (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of left tibia (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of right tibia (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of thoracic vertebra Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of bilateral femurs (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of bilateral femurs (disorder) Associated morphology True Osteolysis Inferred relationship Some 2
Osteolysis of left radius (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of right radius (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of bilateral radii Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of bilateral radii Associated morphology True Osteolysis Inferred relationship Some 2
Osteolysis of bilateral feet Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of bilateral feet Associated morphology True Osteolysis Inferred relationship Some 2
Osteolysis of bilateral tibias Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of bilateral tibias Associated morphology True Osteolysis Inferred relationship Some 2
Osteolysis of acromial end of bilateral clavicles Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of acromial end of bilateral clavicles Associated morphology True Osteolysis Inferred relationship Some 2
Osteolysis of tibia Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of humerus (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of radius Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of femur (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of left femur Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of right femur (disorder) Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of acromial end of clavicle Associated morphology True Osteolysis Inferred relationship Some 1
Osteolysis of foot Associated morphology True Osteolysis Inferred relationship Some 1

Reference Sets

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