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25723000: Dysplasia (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
43110010 Dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
756074016 Dysplasia (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1080891000241117 dysplasie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

38 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dysplasia Is a Growth alteration true Inferred relationship Some
Dysplasia Is a Lesion (morphologic abnormality) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hallermann-Streiff syndrome Associated morphology False Dysplasia Inferred relationship Some 1
Bronchopulmonary dysplasia of newborn (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
Severe biliary tract dysplasia (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
Dysplasia of extrahepatic bile ducts (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
Mitral leaflet dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Frontonasal dysplasia sequence Associated morphology True Dysplasia Inferred relationship Some 1
Diffuse fibroadenosis of breast Associated morphology True Dysplasia Inferred relationship Some 1
Dysplasia of anus (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
Arteriohepatic dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Benign mammary dysplasia NOS Associated morphology False Dysplasia Inferred relationship Some 1
Chronic fibroadenosis of breast Associated morphology True Dysplasia Inferred relationship Some 1
Mild biliary tract dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Dysplasia of blood vessel of kidney (disorder) Associated morphology False Dysplasia Inferred relationship Some 1
Dysplasia of blood vessel of kidney (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
Fibrous dysplasia of jaw Associated morphology False Dysplasia Inferred relationship Some 1
Dysplastic oral leucoplakia Associated morphology True Dysplasia Inferred relationship Some 2
Dysplasia of prostate (disorder) Associated morphology False Dysplasia Inferred relationship Some 1
Dysplasia of testis (disorder) Associated morphology False Dysplasia Inferred relationship Some 1
Low grade dysplastic nodule (morphologic abnormality) Is a False Dysplasia Inferred relationship Some
High grade dysplastic nodule (morphologic abnormality) Is a False Dysplasia Inferred relationship Some
Dysplasia of testis (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
Dysplasia of prostate (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
Tricuspid leaflet dysplasia Associated morphology False Dysplasia Inferred relationship Some 1
Dysplastic nodule (morphologic abnormality) Is a True Dysplasia Inferred relationship Some
Tricuspid leaflet dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Dysplasia of glottis (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
Fibrous dysplasia of bone with intramuscular myxoma Associated morphology False Dysplasia Inferred relationship Some 2
Enamel dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Hypophosphataemic rickets with nephrotic-glycosuric dwarfism Associated morphology True Dysplasia Inferred relationship Some 2
Temporo-auro-mandibular dysostosis Associated morphology True Dysplasia Inferred relationship Some 2
Achondrogenesis, type IA Associated morphology True Dysplasia Inferred relationship Some 2
Carpotarsal osteochondromatosis is a very rare primary bone dysplasia disorder with characteristics of abnormal bone proliferation and osteochondromas in the upper and lower limbs. Associated morphology True Dysplasia Inferred relationship Some 2
Atelosteogenesis/diastrophic dysplasia Associated morphology False Dysplasia Inferred relationship Some 2
Madelung's deformity (disorder) Associated morphology True Dysplasia Inferred relationship Some 3
Adult GM1 gangliosidosis Associated morphology True Dysplasia Inferred relationship Some 2
Enchondromatosis Associated morphology True Dysplasia Inferred relationship Some 2
Spondyloenchondromatosis with basal ganglia calcification (disorder) Associated morphology True Dysplasia Inferred relationship Some 2
Grebe syndrome Associated morphology True Dysplasia Inferred relationship Some 2
Bruck syndrome Associated morphology True Dysplasia Inferred relationship Some 2
Fibrous dysplasia Associated morphology False Dysplasia Inferred relationship Some 2
Naso-maxillary dysostosis Associated morphology True Dysplasia Inferred relationship Some 2
Achondrogenesis, type IB Associated morphology True Dysplasia Inferred relationship Some 2
Cranioectodermal dysplasia Associated morphology True Dysplasia Inferred relationship Some 2
Osteomesopyknosis is a very rare benign bone disorder characterized by bone dysplasia manifested by patchy sclerosis of the axial skeleton and increased bone mineral content. Associated morphology False Dysplasia Inferred relationship Some 2
Otomandibular dysostosis Associated morphology True Dysplasia Inferred relationship Some 3
Cole-Carpenter dysplasia (disorder) Associated morphology True Dysplasia Inferred relationship Some 2
A rare disorder characterised by increased bone density (predominantly diaphyseal) and aregenerative corticosteroid-sensitive anaemia. The exact prevalence is unknown. Associated with mutations in the TBXAS1 gene (which encodes thromboxane synthase). Transmitted as an autosomal recessive trait. Associated morphology True Dysplasia Inferred relationship Some 2
Multiple congenital exostosis Associated morphology True Dysplasia Inferred relationship Some 2
Oculodento-osseous dysplasia Associated morphology True Dysplasia Inferred relationship Some 2
Craniometaphyseal dysplasia - severe type Associated morphology True Dysplasia Inferred relationship Some 3
Brachyolmia Associated morphology False Dysplasia Inferred relationship Some 2
Achondroplasia Associated morphology True Dysplasia Inferred relationship Some 3
Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta Associated morphology True Dysplasia Inferred relationship Some 3
Fronto-naso-ethmoidal dysostosis Associated morphology True Dysplasia Inferred relationship Some 3
Brachyrachia (short spine dysplasia) Associated morphology False Dysplasia Inferred relationship Some 2
pseudochondroplasie Associated morphology False Dysplasia Inferred relationship Some 2
Acrodysostosis Associated morphology True Dysplasia Inferred relationship Some 4
Atelosteogenesis type 2 Associated morphology False Dysplasia Inferred relationship Some 2
Achondrogenesis, type II Associated morphology True Dysplasia Inferred relationship Some 2
Shwachman syndrome Associated morphology True Dysplasia Inferred relationship Some 3
A lysosomal storage disease with characteristics of coarse facial features, macular cherry red spot, and dysostosis multiplex. Clinical presentation can be heterogeneous ranging from a severe, early-onset, rapidly progressive infantile form to late onset, slowly progressive juvenile/adult form. Associated morphology True Dysplasia Inferred relationship Some 2
Saldino-Mainzer dysplasia Associated morphology True Dysplasia Inferred relationship Some 3
Craniometaphyseal dysplasia - mild type Associated morphology True Dysplasia Inferred relationship Some 3
Congenital glenoid dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Madelung's deformity (disorder) Associated morphology True Dysplasia Inferred relationship Some 2
Spheno-frontal dysostosis Associated morphology True Dysplasia Inferred relationship Some 2
Temporo-aural dysostosis Associated morphology True Dysplasia Inferred relationship Some 2
Frontal dysostosis Associated morphology False Dysplasia Inferred relationship Some 2
Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta Associated morphology True Dysplasia Inferred relationship Some 2
Hyperphosphatasemia tarda Associated morphology True Dysplasia Inferred relationship Some 3
Fronto-naso-ethmoidal dysostosis Associated morphology True Dysplasia Inferred relationship Some 2
Maffucci syndrome Associated morphology True Dysplasia Inferred relationship Some 3
Oculodento-osseous dysplasia - severe type Associated morphology False Dysplasia Inferred relationship Some 7
Hay-Wells syndrome of ectodermal dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Oculodentodigital syndrome Associated morphology True Dysplasia Inferred relationship Some 1
Oculodento-osseous dysplasia - mild type (disorder) Associated morphology False Dysplasia Inferred relationship Some 7
Oculodentodigital syndrome Associated morphology True Dysplasia Inferred relationship Some 4
Congenital pulmonary lymphatic dysplasia syndrome (disorder) Associated morphology False Dysplasia Inferred relationship Some 2
Congenital pulmonary acinar dysplasia Associated morphology False Dysplasia Inferred relationship Some 2
Dysplasia of cementum (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
Hemimaxillofacial dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Anhidrotic ectodermal dysplasia with immune deficiency (disorder) Associated morphology False Dysplasia Inferred relationship Some 2
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology False Dysplasia Inferred relationship Some 4
Hidrotic ectodermal dysplasia syndrome Associated morphology False Dysplasia Inferred relationship Some 4
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Associated morphology False Dysplasia Inferred relationship Some 4
Hypohidrotic X-linked ectodermal dysplasia Associated morphology False Dysplasia Inferred relationship Some 4
Ectrodactyly-ectodermal dysplasia-clefting syndrome Associated morphology False Dysplasia Inferred relationship Some 7
Anhidrotic ectodermal dysplasia with immune deficiency (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
Ectrodactyly-ectodermal dysplasia-clefting syndrome Associated morphology True Dysplasia Inferred relationship Some 1
Renal dysplasia due to fetal exposure to angiotensin converting enzyme inhibitor Associated morphology True Dysplasia Inferred relationship Some 2
Retinal dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Geographic retinal dysplasia Associated morphology False Dysplasia Inferred relationship Some 3
A rare genetic eye disease characterized by abnormal proliferation of retinal tissue resulting in the formation of retinal folds, thereby causing gliosis and, clinically, variable degrees of visual impairment. No clinical findings other than those associated with the eyes have been demonstrated. Associated morphology False Dysplasia Inferred relationship Some 3
Dysplasia of trochlea of femur (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
An uncommon transitory hair shaft dysplasia characterized by segmental duplication of the hair shaft: a ramification generates two parallel branches which fuse to form a single shaft again. Each branch is covered by its own cuticle. Associated morphology True Dysplasia Inferred relationship Some 1
arthrose de la hanche concomitante de et due à une dysplasie Associated morphology False Dysplasia Inferred relationship Some 1
Bilateral multicystic renal dysplasia (disorder) Associated morphology True Dysplasia Inferred relationship Some 2
Fibrous dysplasia of orbit (disorder) Associated morphology False Dysplasia Inferred relationship Some 2
Fibroadenosis of bilateral breasts (disorder) Associated morphology True Dysplasia Inferred relationship Some 3
Fibroadenosis of bilateral breasts (disorder) Associated morphology True Dysplasia Inferred relationship Some 4
Congenital dysplasia of tricuspid valve Associated morphology True Dysplasia Inferred relationship Some 1

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