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Translation of "warm type " (English → French) :
TERMINOLOGY
see also In-Context Translations below Primary (idiopathic) warm autoimmune hemolytic anemia
anémie hémolytique auto-immune chaude primaire (idiopathique)
SNOMEDCT-BE (idiopathic) warm autoimmune hemolytic anemia / 127051003
SNOMEDCT-BE (idiopathique) / 127051003
Bedpan warming cabinet
armoire chauffante pour bassin de lit
SNOMEDCT-BE (physical object) / 466483006
SNOMEDCT-BE (physical object) / 466483006
Infant incubator warming hood
couvercle chauffant de couveuse pour bébé
SNOMEDCT-BE (physical object) / 470524005
SNOMEDCT-BE (physical object) / 470524005
Secondary warm autoimmune hemolytic anemia
anémie hémolytique auto-immune chaude secondaire
SNOMEDCT-BE (disorder) / 127052005
SNOMEDCT-BE (disorder) / 127052005
AIHA - Warm autoimmune hemolytic anemia
anémie hémolytique auto-immune chaude
SNOMEDCT-BE (disorder) / 3978000
SNOMEDCT-BE (disorder) / 3978000
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
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'warm type'
Date index:2022-01-22 -
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