All diseases

OMIM ID
253800
OMIM term:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4
Alternative terms:
FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY; FCMD
WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, FKTN-RELATED
(∗) Location:
9q31.2  
(†) Associated OMIM genes:
FKTN  
(‡) Associated MGI genes:
Fktn  

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