All diseases

OMIM ID
158350
OMIM term:
COWDEN DISEASE; CD
Alternative terms:
COWDEN SYNDROME; CS
MULTIPLE HAMARTOMA SYNDROME; MHAM DYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED
CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED
CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED
LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED
PROTEUS-LIKE SYNDROME, INCLUDED
(∗) Location:
10q23.31  
(†) Associated OMIM genes:
PTEN  
(‡) Associated MGI genes:
Pten  

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