syndromic disease
47,XYY syndrome
https://github.com/monarch-initiative/mondo/issues/3155
NCIT:C85237
disomy Y
SCTID:50749006
47,XYY syndrome
47,XYY
MESH:C535317
47, XYY syndrome is a sex chromosome aneuploidy where males receive an additional Y chromosome, and is characterized clinically by tall stature evident from childhood, macrocephaly, facial features (mild hypertelorism, low set ears, a mildly flat malar region), speech delay and an increased risk for social and emotional difficulties, attention deficit hyperactive disorder and autistic spectrum disorder.
Double Y syndrome
Orphanet:8
MedDRA:10056894
YY syndrome
47, XYY syndrome
NORD:1871
Y disomy
Double Y
MONDO:0019339
XYY karyotype
GARD:5674
XYY syndrome
chromosome Y disorder
trisomy