All diseases

OMIM ID
248190
OMIM term:
HYPOMAGNESEMIA 5, RENAL, WITH OCULAR INVOLVEMENT; HOMG5
Alternative terms:
HYPOMAGNESEMIA, RENAL, WITH OCULAR INVOLVEMENT
HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA, NEPHROCALCINOSIS, AND SEVERE OCULAR INVOLVEMENT
FHHNC WITH SEVERE OCULAR INVOLVEMENT
MACULAR COLOBOMA, BILATERAL, WITH HYPERCALCIURIA
(∗) Location:
1p34.2  
(†) Associated OMIM genes:
CLDN19  
(‡) Associated MGI genes:

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