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Autoimmune pancreatitis type 1
Intellectual disability Buenos Aires type
Juvenile sulfatidosis Austin type

Translation of "types veneers " (English → French) :

Dental veneer, custom-made

facette dentaire sur mesure
SNOMEDCT-BE (physical object) / 468756000
SNOMEDCT-BE (physical object) / 468756000


A group of tyrosine related oculocutaneous albinism (OCA1) that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS). The phenotypic spectrum seen in OCA1 i

albinisme oculo-cutané type 1
SNOMEDCT-BE (OCA1) that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS). The phenotypic spectrum seen in OCA1 i / 765146000
SNOMEDCT-BE (disorder) / 765146000


Charcot-Marie-Tooth disease, type 4B2 (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso

maladie de Charcot-Marie-Tooth type 4B2
SNOMEDCT-BE (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso / 715800000
SNOMEDCT-BE (disorder) / 715800000


A rare multiple malformation syndrome with characteristics of severe intrauterine growth retardation, severe microcephaly with a sloping forehead, severe ichthyosis (collodion baby type), and facial dysmorphism. Severe central nervous system defects

syndrome de Neu-Laxova
SNOMEDCT-BE (collodion baby type), and facial dysmorphism. Severe central nervous system defects / 77817004
SNOMEDCT-BE (disorder) / 77817004


This syndrome has characteristics of Hirschsprung disease and absence or hypoplasia of the nails and distal phalanges of the thumbs and great toes (type D brachydactyly). It has been described in four males from one family (two brothers and two mater

syndrome de maladie de Hirschsprung-brachydactylie type D
SNOMEDCT-BE (type D brachydactyly). It has been described in four males from one family (two brothers and two mater / 721222007
SNOMEDCT-BE (disorder) / 721222007


Classical mycosis fungoides is the most common type of mycosis fungoides, a form of cutaneous T-cell lymphoma, and is characterised by slow progression from patches to more infiltrated plaques and eventually to tumours. The disease first manifests by

mycosis fongoïde classique
SNOMEDCT-BE (disorder) / 765328000
SNOMEDCT-BE (disorder) / 765328000


Juvenile sulfatidosis Austin type

déficit multiple en sulfatases
SNOMEDCT-BE (disorder) / 54898003
SNOMEDCT-BE (disorder) / 54898003


Autoimmune pancreatitis type 1

pancréatite auto-immune type 1
SNOMEDCT-BE (disorder) / 722872000
SNOMEDCT-BE (disorder) / 722872000


Intellectual disability Buenos Aires type

déficience intellectuelle type Buenos-Aires
SNOMEDCT-BE (disorder) / 725906006
SNOMEDCT-BE (disorder) / 725906006


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

omodysplasie
SNOMEDCT-BE / 725164008
SNOMEDCT-BE (disorder) / 725164008




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'types veneers'

Date index:2021-05-11 -

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