HGQN - Krankheit

Krankheit

Cowden-Syndrom

COWDEN DISEASE; CD

OMIM: 158350

Synonyme

CS

COWDEN SYNDROME; CS
MULTIPLE HAMARTOMA SYNDROME; MHAM

Gen locations

AKT1(OMIM 164730)
KLLN(OMIM 612105)
PIK3CA(OMIM 171834)
PTEN(OMIM 601728)
SDHB(OMIM 185470)
SDHC(OMIM 602413)
SDHD(OMIM 602690)