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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
Atelosteogenesis type 2 Associated morphology True Dysplasia Inferred relationship Some 1
Omodysplasia I Associated morphology False Dysplasia Inferred relationship Some 1
Omodysplasia II Associated morphology False Dysplasia Inferred relationship Some 1
Pseudodiastrophic dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Otospondylomegaepiphyseal dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Achondrogenesis, type II Associated morphology False Dysplasia Inferred relationship Some 1
Spondylometaphyseal dysplasia - Sutcliffe type Associated morphology True Dysplasia Inferred relationship Some 1
Spondyloenchondrodysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Epiphyseal dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Chondrodysplasia punctata, X-linked recessive type (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
Chondrodysplasia punctata, MT type Associated morphology True Dysplasia Inferred relationship Some 1
Metaphyseal chondrodysplasia, Spahr type Associated morphology True Dysplasia Inferred relationship Some 1
Metaphyseal anadysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Brachyrachia (short spine dysplasia) Associated morphology False Dysplasia Inferred relationship Some 1
Acromicric dysplasia Associated morphology False Dysplasia Inferred relationship Some 1
Saldino-Mainzer dysplasia Associated morphology False Dysplasia Inferred relationship Some 1
Dysplasias with significant membranous bone involvement Associated morphology True Dysplasia Inferred relationship Some 1
Multiple dislocations with dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
dysplasie spondylo-épimétaphysaire avec hyperlaxité ligamentaire Associated morphology False Dysplasia Inferred relationship Some 1
Osteodysplastic primordial dwarfism Associated morphology True Dysplasia Inferred relationship Some 1
Osteodysplastic primordial dwarfism, type 1 Associated morphology True Dysplasia Inferred relationship Some 1
Osteodysplastic primordial dwarfism, type 2 Associated morphology False Dysplasia Inferred relationship Some 1
Dysplasia with decreased bone density Associated morphology True Dysplasia Inferred relationship Some 1
Osteogenesis imperfecta type IIA presents with broad ribs with multiple fractures, continuous beaded ribs and severe under-modeling of the femur. Associated morphology True Dysplasia Inferred relationship Some 1
Geroderma osteodysplastica Associated morphology False Dysplasia Inferred relationship Some 1
Dysplasia with defective mineralization Associated morphology True Dysplasia Inferred relationship Some 1
Dysplasia with increased bone density Associated morphology True Dysplasia Inferred relationship Some 1
Osteosclerosis - Stanescu type Associated morphology True Dysplasia Inferred relationship Some 1
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 True Dysplasia Inferred relationship Some 1
Osteomesopycnosis Associated morphology False Dysplasia Inferred relationship Some 1
Osteopathia striata with cranial sclerosis Associated morphology True Dysplasia Inferred relationship Some 1
Pachydermoperiostosis - familial Associated morphology True Dysplasia Inferred relationship Some 1
Oculodento-osseous dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Oculodento-osseous dysplasia - severe type Associated morphology True Dysplasia Inferred relationship Some 2
Oculodento-osseous dysplasia - mild type (disorder) Associated morphology True Dysplasia Inferred relationship Some 2
Disorganised development of cartilaginous and fibrous components of the skeleton Associated morphology True Dysplasia Inferred relationship Some 1
Dyschondroplasia Associated morphology False Dysplasia Inferred relationship Some 1
Fibrous dysplasia Associated morphology False Dysplasia Inferred relationship Some 1
Infantile myofibromatosis Associated morphology False Dysplasia Inferred relationship Some 1
Idiopathic osteolyses Associated morphology False Dysplasia Inferred relationship Some 1
Neurofibromatosis type 3 Associated morphology False Dysplasia Inferred relationship Some 2
Ash leaf spot, tuberous sclerosis (disorder) Associated morphology False Dysplasia Inferred relationship Some 2
Shagreen patch Associated morphology False Dysplasia Inferred relationship Some 3
Giant fibroadenoma of breast Associated morphology False Dysplasia Inferred relationship Some 3
Juvenile fibroadenoma of breast Associated morphology False Dysplasia Inferred relationship Some 3
Adenocarcinoma in situ of cervix Associated morphology False Dysplasia Inferred relationship Some 2
Solitary cyst of breast Associated morphology False Dysplasia Inferred relationship Some 2
Enchondromatosis Associated morphology True Dysplasia Inferred relationship Some 1
Idiopathic hyperphosphatasemia Associated morphology False Dysplasia Inferred relationship Some 1
Osteogenesis imperfecta, perinatal lethal (disorder) Associated morphology False Dysplasia Inferred relationship Some 1
Spondylodysplastic group Associated morphology True Dysplasia Inferred relationship Some 1
Short rib dysplasia group (with or without polydactyly) Associated morphology False Dysplasia Inferred relationship Some 1
Kniest-Stickler dysplasia group Associated morphology False Dysplasia Inferred relationship Some 1
Spondyloepiphyseal dysplasia congenita Associated morphology True Dysplasia Inferred relationship Some 1
Chondrodysplasia punctata (stippled epiphyses) group (disorder) Associated morphology True Dysplasia Inferred relationship Some 1
Bent bone dysplasia group Associated morphology True Dysplasia Inferred relationship Some 1
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism type I Associated morphology False Dysplasia Inferred relationship Some 1
Sialic storage disease Associated morphology True Dysplasia Inferred relationship Some 1
Dysostosis multiplex group Associated morphology True Dysplasia Inferred relationship Some 1
Acromesomelic dysplasia syndrome Associated morphology True Dysplasia Inferred relationship Some 1
Osteogenesis imperfecta, type IV B Associated morphology True Dysplasia Inferred relationship Some 1
Osteogenesis imperfecta, type IV A Associated morphology True Dysplasia Inferred relationship Some 1
Cervical intraepithelial neoplasia (disorder) Associated morphology False Dysplasia Inferred relationship Some 1
Cervical intraepithelial neoplasia grade 1 Associated morphology False Dysplasia Inferred relationship Some 1
Cervical intraepithelial neoplasia grade 2 Associated morphology False Dysplasia Inferred relationship Some 1
Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency Associated morphology False Dysplasia Inferred relationship Some 1
Mild stomach dysplasia Associated morphology False Dysplasia Inferred relationship Some 1
Moderate stomach dysplasia Associated morphology False Dysplasia Inferred relationship Some 1
Severe stomach dysplasia Associated morphology False Dysplasia Inferred relationship Some 1
Dysostosis of bone of skull Associated morphology True Dysplasia Inferred relationship Some 1
Melnick-Needles syndrome Associated morphology True Dysplasia Inferred relationship Some 1
Hypoplastic chondrodystrophy Associated morphology True Dysplasia Inferred relationship Some 1
Autosomal recessive lethal osteopetrosis Associated morphology False Dysplasia Inferred relationship Some 1
chondrodysplasie ponctuée congénitale Associated morphology False Dysplasia Inferred relationship Some 1
Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts Associated morphology False Dysplasia Inferred relationship Some 1
Vascular Ehlers-Danlos syndrome Associated morphology False Dysplasia Inferred relationship Some 1
Sclerosteosis Associated morphology True Dysplasia Inferred relationship Some 1
Mohr syndrome Associated morphology False Dysplasia Inferred relationship Some 1
Juvenile GM1 gangliosidosis Associated morphology True Dysplasia Inferred relationship Some 1
Schinzel-Giedion syndrome Associated morphology True Dysplasia Inferred relationship Some 1
Neurofibromatosis syndrome Associated morphology False Dysplasia Inferred relationship Some 2
Occipital dysplasia Associated morphology False Dysplasia Inferred relationship Some 2
Sturge-Weber syndrome Associated morphology False Dysplasia Inferred relationship Some 1
syndrome d'Ehlers-Danlos type 2 Associated morphology False Dysplasia Inferred relationship Some 1
Gastric dysplasia Associated morphology False Dysplasia Inferred relationship Some 1
Periodic fibroadenosis of breast Associated morphology False Dysplasia Inferred relationship Some 1
A rare hereditary patellar dysostosis characterised by nail hypoplasia or aplasia, aplastic or hypoplastic patellae, elbow dysplasia, and the presence of iliac horns as well as renal and ocular anomalies. Associated morphology False Dysplasia Inferred relationship Some 1
Chondrodysplasia punctata, Conradi-Hünermann type Associated morphology False Dysplasia Inferred relationship Some 1
Ehlers-Danlos syndrome Associated morphology False Dysplasia Inferred relationship Some 1
Fibroadenosis of breast Associated morphology False Dysplasia Inferred relationship Some 1
Metaphyseal chondrodysplasia, Jansen type Associated morphology True Dysplasia Inferred relationship Some 1
Infantile cortical hyperostosis (disorder) Associated morphology False Dysplasia Inferred relationship Some 1
Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome Associated morphology False Dysplasia Inferred relationship Some 1
Ehlers-Danlos syndrome, hydroxylysine-deficient Associated morphology False Dysplasia Inferred relationship Some 1
Bone island Associated morphology False Dysplasia Inferred relationship Some 1
Ectopic bone tissue, congenital Associated morphology False Dysplasia Inferred relationship Some 1
Senter syndrome Associated morphology True Dysplasia Inferred relationship Some 1
Robinson nail dystrophy-deafness syndrome Associated morphology False Dysplasia Inferred relationship Some 1
Temporomandibular dysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Metaphyseal chondrodysplasia Associated morphology True Dysplasia Inferred relationship Some 1
Weill-Marchesani syndrome (disorder) Associated morphology False Dysplasia Inferred relationship Some 1

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This concept is not in any reference sets

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