All diseases

OMIM ID
610127
OMIM term:
CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10
Alternative terms:
CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT
NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY NEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED
(∗) Location:
11p15.5  
(†) Associated OMIM genes:
CTSD  
(‡) Associated MGI genes:
Ctsd  

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