Concept information
Clinical finding (finding)
Musculoskeletal system finding
Disease of the musculoskeletal system, NOS
Congenital anomaly of musculoskeletal system
Preferred term
Skeletal dysplasia
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- 3-M syndrome
- Angel-shaped phalangoepiphyseal dysplasia (disorder)
- Autoinflammatory disease due to interleukin-1 receptor antagonist deficiency
- Ballard syndrome (disorder)
- Benallegue Lacete syndrome
- Bent bone dysplasia group
- Brachydactyly elbow wrist dysplasia (disorder)
- Camptodactyly syndrome Guadalajara type 2 (disorder)
- Chondrodysplasia punctata
- Congenital glenoid dysplasia
- Congenital hip dysplasia
- Coxoauricular syndrome (disorder)
- Craniofacial conodysplasia syndrome (disorder)
- Craniofrontonasal dysplasia (disorder)
- Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome (disorder)
- Deafness with skeletal dysplasia and lip granuloma syndrome (disorder)
- Defects of tubular bones and spine (disorder)
- Dysostosis
- Dysplasias with significant membranous bone involvement
- Dysplasia with increased bone density
- Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder)
- Familial osteodysplasia Anderson type (disorder)
- Frank-Ter Haar syndrome (disorder)
- Heart defect and limb shortening syndrome (disorder)
- Heide syndrome
- Immunodeficiency, short limb dwarfism syndrome
- Intellectual disability, balding, patella luxation, acromicria syndrome (disorder)
- Lethal occipital encephalocele, skeletal dysplasia syndrome (disorder)
- Lipodystrophy, intellectual disability, deafness syndrome (disorder)
- MCAHS (multiple congenital anomalies, hypotonia, seizures syndrome) type 3
- Mesomelic dysplasia
- Metaphyseal chondrodysplasia
- Metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome (disorder)
- Microspherophakia with metaphyseal dysplasia syndrome (disorder)
- Mononen Karnes Senac syndrome
- Omodysplasia (disorder)
- Osteocraniostenosis (disorder)
- Osteogenesis imperfecta
- Osteosclerosis - Stanescu type
- Otopalatodigital syndrome spectrum disorder
- Parietal foramina with clavicular hypoplasia
- Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (disorder)
- Pyknoachondrogenesis (disorder)
- Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder)
- Rhizomelic dysplasia of Patterson Lowry type (disorder)
- Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome
- Skeletal dysplasia with epilepsy and short stature syndrome (disorder)
- SOFT syndrome
- Spondyloepiphyseal dysplasia congenita
- Spondylometaphyseal dysplasia
- Spondyloperipheral dysplasia (disorder)
- Tarsal-carpal coalition syndrome
- Thin ribs, tubular bones, dysmorphism syndrome
Associated morphology
Finding site
Is a
Occurrence
Pathological process
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/105986008
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}