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

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

'pulpal dysplasia' ->

Date index: 2022-06-08