All diseases

OMIM ID
309000
OMIM term:
LOWE OCULOCEREBRORENAL SYNDROME; OCRL
Alternative terms:
OCRL1
LOWE SYNDROME
PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE 5-PHOSPHATASE DEFICIENCY
(∗) Location:
Xq25-q26  
(†) Associated OMIM genes:
OCRL  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/jpex78p4