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Familial CD8 deficiency
Familial apolipoprotein C-II deficiency
Familial high density lipoprotein deficiency
Rickets
Tangier disease
Tangier's disease

Translation of "Familial CD8 deficiency " (English → French) :

Familial CD8 deficiency

susceptibilité aux infections respiratoires associée à une mutation de la chaîne alpha de CD8
SNOMEDCT-BE (disorder) / 766983005
SNOMEDCT-BE (disorder) / 766983005


Abetalipoproteinaemia High-density lipoprotein deficiency Hypoalphalipoproteinaemia Hypobetalipoproteinaemia (familial) Lecithin cholesterol acyltransferase deficiency Tangier disease

Abêtalipoprotéinémie Déficit en:lécithine-cholestérol-acyltransférase | lipoprotéines de haute densité | Hypoalphalipoprotéinémie Hypobêtalipoprotéinémie Maladie de Tangier
WORLD HEALTH ORGANIZATION ICD-10: E78.6
WORLD HEALTH ORGANIZATION ICD-10: E78.6


Tangier's disease | Tangier disease | familial high density lipoprotein deficiency

maladie de Tangier | a-alphalipoprotéinémie
médecine > sémiologie et pathologie
médecine > sémiologie et pathologie


A syndrome with characteristics of immune deficiency and neurological disorders in females and neonatal death in males. The syndrome has been described in only one family with nine affected individuals (five males and four females) spanning two gener

syndrome immuno-neurologique lié à l'X
SNOMEDCT-BE (five males and four females) spanning two gener / 719827008
SNOMEDCT-BE (disorder) / 719827008


Familial apolipoprotein C-II deficiency

déficit familial en apoC-II
SNOMEDCT-BE (disorder) / 33513003
SNOMEDCT-BE (disorder) / 33513003


Acid phosphatase deficiency Familial hypophosphataemia Hypophosphatasia Vitamin-D-resistant:osteomalacia | rickets

Déficit en phosphatase acide Hypophosphatasie Hypophosphatémie familiale Ostéomalacie résistante à la vitamine D Rachitisme résistant à la vitamine D
WORLD HEALTH ORGANIZATION ICD-10: E83.3
WORLD HEALTH ORGANIZATION ICD-10: E83.3




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'Familial CD8 deficiency'

Date index:2024-01-30 -

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