All diseases

OMIM ID
162350
OMIM term:
CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B
Alternative terms:
KUFS DISEASE, AUTOSOMAL DOMINANT
CEROID LIPOFUSCINOSIS, NEURONAL, PARRY TYPE
(∗) Location:
20q13.33  
(†) Associated OMIM genes:
DNAJC5  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/nv2gesgd