All diseases

OMIM ID
236670
OMIM term:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1
Alternative terms:
WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT1-RELATED
HYDROCEPHALUS, AGYRIA, AND RETINAL DYSPLASIA
HARD SYNDROME
CEREBROOCULAR DYSPLASIA-MUSCULAR DYSTROPHY SYNDROME
COD-MD SYNDROME
(∗) Location:
9q34.13  
(†) Associated OMIM genes:
POMT1  
(‡) Associated MGI genes:
Col4a1  

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