All diseases

OMIM ID
270700
OMIM term:
SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15
Alternative terms:
SPASTIC PARAPLEGIA AND RETINAL DEGENERATION
KJELLIN SYNDROME
(∗) Location:
14q24.1  
(†) Associated OMIM genes:
ZFYVE26  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/4swvqub5