A rare genetic immuno-osseous dysplasia disorder with characteristics of pre and post-natal growth retardation, hypotonia, borderline to moderate intellectual disability, retinal dystrophy, spondyloepiphyseal dysplasia (epiphyseal dysplasia, epiphyse

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

spondylo-epifyseale dysplasie, retinale dystrofie, immuundeficiëntie

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

dysplasia | abnormality of development

http://users.ugent.be/~rvdstic (...) (...) [HTML] [2018-01-01]

dysplasie | ongewone ontwikkeling

http://users.ugent.be/~rvdstic (...) (...) [HTML] [2018-01-01]

http://users.ugent.be/~rvdstic (...) [HTML] [2018-01-01]

cleidocranial dysostosis,cleidocranial dysplasia

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

cleidocranialiasis | dysostosis cleidocranialis

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

Omodysplasia is a rare skeletal dysplasia characterised by severe limb shortening and facial dysmorphism. Two types of omodysplasia have been described: an autosomal recessive or generalised form (also referred to as micromelic dysplasia with disloca

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

omodysplasie

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Anderen hebben gezocht naar : pulpal dysplasia pulpal gangrene pulpal abscess pulpitis acute pyle's disease siemens'syndrome abnormality of development chronic congenital ectodermal dysplasia craniometaphyseal dysplasia dysplasia ectodermal dysplasia metaphyseal dysplasia stones suppurative Pulpal dysplasia

datacenter (1): www.wordscope.be (v4.0.br)

'Pulpal dysplasia' ->

Date index: 2023-07-26