All diseases

OMIM ID
268200
OMIM term:
MYOGLOBINURIA, ACUTE RECURRENT, AUTOSOMAL RECESSIVE
Alternative terms:
MYOGLOBINURIA, FAMILIAL PAROXYSMAL PARALYTIC
RHABDOMYOLYSIS, ACUTE RECURRENT
(∗) Location:
2p25.1  
(†) Associated OMIM genes:
LPIN1  
(‡) Associated MGI genes:

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