Concept information
Preferred term
Hereditary disorder of musculoskeletal system
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Acromicric dysplasia
- Atelosteogenesis
- Choanal atresia with radial ray hypoplasia
- Chondrodysplasia punctata, X-linked recessive type
- Chronic infantile neurological, cutaneous and articular syndrome
- Craniodiaphyseal dysplasia
- Curry-Hall syndrome
- Desbuquois syndrome
- Diaphragmatic defect, limb deficiency, skull defect syndrome (disorder)
- Dysostosis multiplex group
- Dysplasia epiphysealis hemimelica
- Genetically determined myasthenia
- Geroderma osteodysplastica
- Glycogen synthase deficiency
- Hereditary progressive muscular dystrophy
- Huntington's chorea
- Hypermobility syndrome
- Keutel syndrome (disorder)
- Lipid storage myopathy
- Mandibuloacral dysostosis
- MERRF - Myoclonic epilepsy - ragged red fibres
- Morquio syndrome
- Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
- Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
- Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (disorder)
- Osteogenesis imperfecta, type IV B
- Osteopathia striata, pigmentary dermopathy, white forelock syndrome
- Osteopetrosis
- Osteosclerosis
- PARC syndrome
- Prune belly syndrome
- Roifman-Melamed syndrome
- Short stature locking fingers syndrome (disorder)
- Spastic paraparesis co-occurrent with deafness (disorder)
Finding site
Is a
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/363212003
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