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