All diseases

OMIM ID
151100
OMIM term:
LEOPARD SYNDROME 1
Alternative terms:
LENTIGINOSIS, CARDIOMYOPATHIC
MULTIPLE LENTIGINES SYNDROME
(∗) Location:
12q24.13  
(†) Associated OMIM genes:
PTPN11  
(‡) Associated MGI genes:
Ptpn11  

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* quick link - http://q.sanger.ac.uk/6xyemi64