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77881008: Osteochondropathy (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
129246013 Osteochondropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
129249018 Disease of bone AND cartilage en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
818760013 Osteochondropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4644351000241118 ostéochondropathie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


90 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteochondropathy Is a Cartilage disorder true Inferred relationship Some
Osteochondropathy Is a Disorder of bone (disorder) true Inferred relationship Some
Osteochondropathy Finding site Cartilaginous tissue structure false Inferred relationship Some
Osteochondropathy Finding site Skeletal system structure false Inferred relationship Some
Osteochondropathy Finding site Bone structure true Inferred relationship Some 1
Osteochondropathy Finding site Cartilage structure (body structure) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Dislocation of arytenoid cartilage (disorder) Is a False Osteochondropathy Inferred relationship Some
Perichondritis of larynx Is a False Osteochondropathy Inferred relationship Some
Chondroradionecrosis of larynx Is a False Osteochondropathy Inferred relationship Some
Calcification of laryngeal cartilage Is a False Osteochondropathy Inferred relationship Some
Congenital abnormal fusion of centrum cartilage of sacral vertebra Is a True Osteochondropathy Inferred relationship Some
Congenital abnormal fusion of centrum cartilage of lumbar vertebra (disorder) Is a True Osteochondropathy Inferred relationship Some
Cleft cartilaginous centrum of sacral vertebra Is a True Osteochondropathy Inferred relationship Some
Cleft cartilaginous centrum of lumbar vertebra Is a True Osteochondropathy Inferred relationship Some
Congenital abnormal fusion of centrum cartilage of thoracic vertebra Is a True Osteochondropathy Inferred relationship Some
Cleft cartilaginous centrum of thoracic vertebra Is a True Osteochondropathy Inferred relationship Some
Degeneration of cervical intervertebral disc co-occurrent with osteophyte of cervical vertebra (disorder) Is a True Osteochondropathy Inferred relationship Some
Degeneration of thoracic intervertebral disc co-occurrent with osteophyte (disorder) Is a True Osteochondropathy Inferred relationship Some
Degeneration of lumbar intervertebral disc co-occurrent with osteophyte of lumbar vertebra (disorder) Is a True Osteochondropathy Inferred relationship Some
Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome is a rare, genetic primary bone dysplasia disorder characterized by disproportionate short stature with shortening of upper and lower limbs, short and broad fingers with short hands, narrowed chest with rib abnormalities and pectus excavatum, abnormal chondral calcifications (including larynx, trachea and costal cartilages) and facial dysmorphism (frontal bossing, hypertelorism, prominent eyes, short flat nose, wide nostrils, high-arched palate, long philtrum). Platyspondyly (especially of cervical spine) and abnormal epiphyses and metaphyses are observed on radiography. Atlantoaxial instability causing spinal compression and recurrent respiratory disease are potential complications that may result lethal. Is a True Osteochondropathy Inferred relationship Some
Dysplasia epiphysealis hemimelica Is a True Osteochondropathy Inferred relationship Some
McCune Albright syndrome (disorder) Is a False Osteochondropathy Inferred relationship Some
Multiple congenital exostosis Is a True Osteochondropathy Inferred relationship Some
A rare primary bone dysplasia characterized by Perthes-like pelvic anomalies (premature closure of the capital femoral epiphyses and widened femoral necks with flattened femoral heads), arthralgias of hips and knees, and occurrence of enchondromata and ecchondromata. There have been no further descriptions in the literature since 1971. Is a True Osteochondropathy Inferred relationship Some
pseudochondroplasie Is a False Osteochondropathy Inferred relationship Some
Enchondromatosis Is a True Osteochondropathy Inferred relationship Some
An association reported in a single kindred characterized by the variable presence of the following features: anetodermia (macular atrophy of the skin), multiple exostoses, and brachydactyly type E. There have been no further descriptions in the literature since 1985. Is a True Osteochondropathy Inferred relationship Some
Polyostotic fibrous dysplasia of bone Is a False Osteochondropathy Inferred relationship Some
Osteoglophonic dysplasia Is a True Osteochondropathy Inferred relationship Some
Metachondromatosis Is a False Osteochondropathy Inferred relationship Some
Carpotarsal osteochondromatosis is a very rare primary bone dysplasia disorder with characteristics of abnormal bone proliferation and osteochondromas in the upper and lower limbs. Is a True Osteochondropathy Inferred relationship Some
Genochondromatosis type 2 is a rare genetic bone development disorder characterized by normal clavicles and symmetrical, generalized metaphyseal enchondromas, particularly in the distal femur, proximal humerus, and bones of the wrists, hands, and feet. Lesions regress later in life with growth cartilage obliteration. Clinical examination is normal and the course of the disease is benign. Is a True Osteochondropathy Inferred relationship Some
A rare primary bone dysplasia characterized by severe intrauterine and postnatal growth retardation and short stature in association with craniofacial dysmorphism (such as large forehead, triangular face, low-set ears, and micro-retrognathism) and osteochondrodysplastic lesions. Radiographic findings include epiphyseal maturation delay, abnormal metaphyses, a narrow thorax, small pelvis, and short and broad metacarpal bones and phalanges. There have been no further descriptions in the literature since 1996. Is a True Osteochondropathy Inferred relationship Some
Fibrous dysplasia Is a False Osteochondropathy Inferred relationship Some
Closed fracture of triradiate cartilage and epiphysis of acetabulum (disorder) Is a False Osteochondropathy Inferred relationship Some

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