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399269003: Arthropathy (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1767189014 Arthropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1778721018 Arthropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786779015 Joint disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786780017 Joint disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786781018 Disorder of joint en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1880831000195115 artropatia it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
302771000077110 arthropathie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
410231000274111 Arthropathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
672071000274112 Gelenkerkrankung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
673451000274119 Gelenkkrankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5373 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Arthropathy (disorder) Is a Disorder of musculoskeletal system (disorder) false Inferred relationship Some
Arthropathy (disorder) Finding site Joint structure true Inferred relationship Some 1
Arthropathy (disorder) Is a Joint finding true Inferred relationship Some
Arthropathy (disorder) Is a Disorder of skeletal system true Inferred relationship Some
Arthropathy (disorder) Is a Disorder of joint region true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Dysplasia of trochlea of femur (disorder) Is a False Arthropathy (disorder) Inferred relationship Some
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. Is a False Arthropathy (disorder) Inferred relationship Some
Triangular fibrocartilage tear Is a False Arthropathy (disorder) Inferred relationship Some
Hydrocephaly-tall stature-joint laxity syndrome is a multiple congenital anomalies syndrome described in two sisters and characterized by the presence of hydrocephalus (onset in infancy), tall stature, joint laxity, and thoracolumbar kyphosis. There have been no further descriptions in the literature since 1989. Is a True Arthropathy (disorder) Inferred relationship Some
Dysmorphism-pectus carinatum-joint laxity syndrome is characterised by joint laxity, pectus carinatum and facial dysmorphism (mild frontal bossing, a beaked nose with a low nasal bridge, malar hypoplasia, chubby cheeks, a striking philtrum and arched upper lips). It has been described in two siblings. The mode of transmission is unknown. Is a True Arthropathy (disorder) Inferred relationship Some
Destruction of joint caused by hemiarthroplasty (disorder) Is a False Arthropathy (disorder) Inferred relationship Some
Isolated sternocostoclavicular hyperostosis is a rare rheumatologic disease characterized by predominantly bilateral, chronic, sterile inflammation and progressive sclerosis and hyperostosis of the sternocostoclavicular joint, with adjacent soft tissue ossification, in the absence of other joint involvement. It presents as recurrent episodes of pain, edema and/or erythema of the sternoclavicular region. Palmoplantar pustulosis may be additionally observed in some cases. Is a False Arthropathy (disorder) Inferred relationship Some
Flexion deformity Is a True Arthropathy (disorder) Inferred relationship Some
Synovial cyst of multiple joints (disorder) Is a False Arthropathy (disorder) Inferred relationship Some
Seropositive rheumatoid arthritis Is a False Arthropathy (disorder) Inferred relationship Some
Seronegative rheumatoid arthritis Is a False Arthropathy (disorder) Inferred relationship Some
Neoplasm of condyle of mandible (disorder) Is a False Arthropathy (disorder) Inferred relationship Some
Mandibular condyle aplasia Is a True Arthropathy (disorder) Inferred relationship Some
Hyperplasia of mandibular condyle Is a True Arthropathy (disorder) Inferred relationship Some
Hypoplasia of mandibular condyle Is a True Arthropathy (disorder) Inferred relationship Some
Deformity of mandibular condyle (disorder) Is a True Arthropathy (disorder) Inferred relationship Some
Slipped distal radial epiphysis Is a False Arthropathy (disorder) Inferred relationship Some
Resorption of mandibular condyle (disorder) Is a True Arthropathy (disorder) Inferred relationship Some
Loose body in joint Is a False Arthropathy (disorder) Inferred relationship Some
Complete epiphyseal arrest of left distal radius (disorder) Is a False Arthropathy (disorder) Inferred relationship Some
Complete epiphyseal arrest of right distal radius (disorder) Is a False Arthropathy (disorder) Inferred relationship Some
Joint formation disorder Is a True Arthropathy (disorder) Inferred relationship Some
De Barsy syndrome (DBS) is characterized by facial dysmorphism (down-slanting palpebral fissures, a broad flat nasal bridge and a small mouth) with a progeroid appearance, large and late-closing fontanel, cutis laxa (CL), joint hyperlaxity, athetoid movements and hyperreflexia, pre- and postnatal growth retardation, intellectual deficit and developmental delay, and corneal clouding and cataract. Is a True Arthropathy (disorder) Inferred relationship Some
Disorder of hip joint (disorder) Is a True Arthropathy (disorder) Inferred relationship Some
Interphalangeal sprain Is a False Arthropathy (disorder) Inferred relationship Some
Nonunion following arthrodesis Is a False Arthropathy (disorder) Inferred relationship Some
Fracture of occipital condyle Is a False Arthropathy (disorder) Inferred relationship Some
Closed fracture involving joint (disorder) Is a False Arthropathy (disorder) Inferred relationship Some
Fracture of condylar process of mandible (disorder) Is a False Arthropathy (disorder) Inferred relationship Some
Fracture of symphysis of mandible (disorder) Is a False Arthropathy (disorder) Inferred relationship Some
Rickets Is a True Arthropathy (disorder) 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 False Arthropathy (disorder) Inferred relationship Some
Lesion of joint Is a True Arthropathy (disorder) Inferred relationship Some
Hypercementosis Is a True Arthropathy (disorder) Inferred relationship Some
Tooth sensitivity at cementoenamel junction Is a True Arthropathy (disorder) Inferred relationship Some
Aplasia of cementum Is a True Arthropathy (disorder) Inferred relationship Some
Loss of lamina dura (disorder) Is a False Arthropathy (disorder) Inferred relationship Some
Synovial hypertrophy of left hand Is a False Arthropathy (disorder) Inferred relationship Some
Synovial hypertrophy of right hand Is a False Arthropathy (disorder) Inferred relationship Some
A rare systemic disease characterized by the association of the features of Ehlers-Danlos syndrome with those of osteogenesis imperfecta. Predominant clinical manifestations include generalized joint hypermobility and dislocations, skin hyperextensibility and/or translucency, easy bruising, and invariable association with mild signs of osteogenesis imperfecta, including short stature, blue sclera, and osteopenia or fractures. Is a True Arthropathy (disorder) Inferred relationship Some
Familial articular hypermobility syndrome (disorder) Is a True Arthropathy (disorder) Inferred relationship Some
Hypertrophy of synovium of joint of hand (disorder) Is a False Arthropathy (disorder) Inferred relationship Some
Localized osteoarthrosis Is a True Arthropathy (disorder) Inferred relationship Some
Exacerbation of osteoarthritis (disorder) Is a True Arthropathy (disorder) Inferred relationship Some
Secondary multiple arthrosis (disorder) Is a True Arthropathy (disorder) Inferred relationship Some
Kashin-Bek disease Is a True Arthropathy (disorder) Inferred relationship Some
Hypertrophy of synovium of left foot Is a True Arthropathy (disorder) Inferred relationship Some
Hypertrophy of synovium of right foot Is a True Arthropathy (disorder) Inferred relationship Some
Chronic musculoskeletal pain due to disorder of joint Due to True Arthropathy (disorder) Inferred relationship Some 3

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