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Syndrome de microdélétion 2p21 sans cystinurie
Syndrome de microdélétion 4q21
Syndrome de microdélétion 8q21.11

Translation of "syndrome de microdélétion 8q21 " (French → English) :

syndrome de microdélétion 8q21.11

Monosomy 8q21.11
SNOMEDCT-BE (disorder) / 718615003
SNOMEDCT-BE (disorder) / 718615003


syndrome de microdélétion 2p21 sans cystinurie

A rare partial autosomal monosomy with characteristics of weak fetal movements, severe infantile hypotonia and feeding difficulties that spontaneously improve with time, urogenital abnormalities (hypospadias or hypoplastic labia majora), global devel
SNOMEDCT-BE (disorder) / 770754006
SNOMEDCT-BE (hypospadias or hypoplastic labia majora), global devel / 770754006


syndrome de microdélétion 4q21

4q21 microdeletion syndrome
SNOMEDCT-BE (disorder) / 719660008
SNOMEDCT-BE (disorder) / 719660008




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syndrome de microdélétion 8q21

Date index:2022-02-06 -

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