bone diseases, developmental

Preferred Label : bone diseases, developmental;

MeSH definition : Diseases resulting in abnormal GROWTH or abnormal MORPHOGENESIS of BONES.;

MeSH synonym : bone disease, developmental; bone dysplasias; dysplasias, bone; dysplasia, bone; bone dysplasia; developmental bone diseases; developmental bone disease;

Details

Origin ID

D001848;

UMLS CUI

C0005941;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Abnormal Bone Development [NCIt concept]
- BONE DEVELOPMENT ABNORMAL [WHO-ART Preferred Term]
- Bone dysplasia [MedDRA LLT]
- Bone dysplasia [PASCAL descriptor]
- Bone dysplasia [Vue CIM-11]
- Cemento-Osseous Dysplasia [NCIt concept]
- Skeletal dysplasia [HPO term]
Currated CISMeF NLP mapping
- Bone Development Disorder [NCIt concept]
- Bone development disorder [MedDRA LLT]
- Disorder of bone development (disorder) [SNOMED CT concept]
- developmental bone disorder [Disease (Nov.)]
Metaterm(s)
- developmental biology and medicine [CISMeF Metaterm]
Record concept(s)
- bone diseases, developmental [MeSH concept]
Related MeSH Supplementary Concept(s)
- CATSHL syndrome [MeSH Supplementary Concept]
- KBG syndrome [MeSH Supplementary Concept]
- Marshall-Smith syndrome [MeSH Supplementary Concept]
- Roifman-Chitayat syndrome [MeSH Supplementary Concept]
- Schwartz-Lelek syndrome [MeSH Supplementary Concept]
- acrocapitofemoral dysplasia [MeSH Supplementary Concept]
- acromesomelic dysplasia, maroteaux type [MeSH Supplementary Concept]
- acromicric dysplasia [MeSH Supplementary Concept]
- agonadism, XY, with mental retardation, short stature, retarded bone age, and multiple extragenital malformations [MeSH Supplementary Concept]
- angel shaped phalangoepiphyseal dysplasia [MeSH Supplementary Concept]
- baby rattle pelvis dysplasia [MeSH Supplementary Concept]
- battaglia neri syndrome [MeSH Supplementary Concept]
- bazopoulou kyrkanidou syndrome [MeSH Supplementary Concept]
- bellini chiumello rimoldi syndrome [MeSH Supplementary Concept]
- bipartite patella [MeSH Supplementary Concept]
- blount disease [MeSH Supplementary Concept]
- bone dysplasia, lethal, holmgren type [MeSH Supplementary Concept]
- brachioskeletogenital syndrome [MeSH Supplementary Concept]
- brachymesomelia renal syndrome [MeSH Supplementary Concept]
- brittle bone disorder [MeSH Supplementary Concept]
- camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia [MeSH Supplementary Concept]
- cervical vertebral dysplasia [MeSH Supplementary Concept]
- cortical defects, wormian bones, and dentinogenesis imperfecta [MeSH Supplementary Concept]
- craniolenticulosutural dysplasia [MeSH Supplementary Concept]
- deafness conductive ptosis skeletal anomalies [MeSH Supplementary Concept]
- diaphragmatic defects, limb deficiencies, and ossification defects of skull [MeSH Supplementary Concept]
- diaphyseal medullary stenosis with malignant fibrous histiocytoma [MeSH Supplementary Concept]
- doughnut lesions of skull, familial [MeSH Supplementary Concept]
- dysplasia epiphysealis hemimelica [MeSH Supplementary Concept]
- dysplasia epiphysealis hemimelica with chondromas and osteochondromas [MeSH Supplementary Concept]
- fountain syndrome [MeSH Supplementary Concept]
- fryns hofkens fabry syndrome [MeSH Supplementary Concept]
- gracile bone dysplasia [MeSH Supplementary Concept]
- gurrieri sammito bellussi syndrome [MeSH Supplementary Concept]
- hall riggs mental retardation syndrome [MeSH Supplementary Concept]
- ischiopatellar dysplasia [MeSH Supplementary Concept]
- kantaputra gorlin syndrome [MeSH Supplementary Concept]
- kozlowski rafinski klicharska syndrome [MeSH Supplementary Concept]
- kozlowski warren fisher syndrome [MeSH Supplementary Concept]
- kyphomelic dysplasia [MeSH Supplementary Concept]
- larsen syndrome, recessive type [MeSH Supplementary Concept]
- lenz majewski hyperostotic dwarfism [MeSH Supplementary Concept]
- lissencephaly type III and bone dysplasia [MeSH Supplementary Concept]
- macroepiphyseal dysplasia, McAlister coe type [MeSH Supplementary Concept]
- membranous cranial ossification, delayed [MeSH Supplementary Concept]
- mesomelic dysplasia, camera type [MeSH Supplementary Concept]
- mesomelic limb shortening and bowing [MeSH Supplementary Concept]
- mononen karnes senac syndrome [MeSH Supplementary Concept]
- osteofibrous dysplasia [MeSH Supplementary Concept]
- osteosclerosis with ichthyosis and premature ovarian failure [MeSH Supplementary Concept]
- patterson pseudoleprechaunism syndrome [MeSH Supplementary Concept]
- pointer syndrome [MeSH Supplementary Concept]
- prenatal bowing [MeSH Supplementary Concept]
- radius absent anogenital anomalies [MeSH Supplementary Concept]
- rhizomelic dysplasia patterson lowry type [MeSH Supplementary Concept]
- rhizomelic dysplasia, scoliosis, and retinitis pigmentosa [MeSH Supplementary Concept]
- rhizomelic syndrome [MeSH Supplementary Concept]
- santos syndrome [MeSH Supplementary Concept]
- short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities [MeSH Supplementary Concept]
- skeletal defects, genital hypoplasia, and mental retardation [MeSH Supplementary Concept]
- skeletal dysplasia and progressive central nervous system degeneration, lethal [MeSH Supplementary Concept]
- skeletal dysplasia with delayed epiphyseal and carpal bone ossification [MeSH Supplementary Concept]
- skeletal dysplasia, rhizomelic, with retinitis pigmentosa [MeSH Supplementary Concept]
- spondyloepimetaphyseal dysplasia, aggrecan type [MeSH Supplementary Concept]
- spranger schinzel myers syndrome [MeSH Supplementary Concept]
- stoll levy francfort syndrome [MeSH Supplementary Concept]
- trichoodontoonychial dysplasia [MeSH Supplementary Concept]
- ulna hypoplasia with mental retardation [MeSH Supplementary Concept]
- vertebral body fusion overgrowth [MeSH Supplementary Concept]
- weismann netter syndrome [MeSH Supplementary Concept]
- wiedemann oldigs oppermann syndrome [MeSH Supplementary Concept]
See also
- connective tissue diseases [MeSH Descriptor]
- growth disorders [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Bone Development Disorder [NCIt concept]
- Bone development disorder [MedDRA LLT]
- Bone dysplasia [MedDRA LLT]
- Disorder of bone development (disorder) [SNOMED CT concept]
- Rare bone development disorder [ORDO Disease]

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