obsolete congenital muscular alpha-dystroglycanopathy with brain and eye anomalies https://github.com/monarch-initiative/mondo/issues/3886 https://github.com/monarch-initiative/mondo/issues/4069 https://rarediseases.info.nih.gov/diseases/12588/congenital-muscular-alpha-dystroglycanopathy-with-brain-and-eye-anomalies https://www.malacards.org/card/congenital_muscular_dystrophy_dystroglycanopathy_type_a true MONDO:0018132 Reason: out of scope. This is an Orphanet grouping class that is considered out of scope for Mondo. Term to consider: muscular dystrophy-dystroglycanopathy' OBSOLETE. Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies (MDDGA) is a cobblestone lissencephaly characterized by and considered to be pathognomonic of a continuum of recessive autosomal disorders with brain, ocular and muscular involvement. MDDGA includes Walker-Warburg syndrome, muscle-eye-brain disease, Fukuyama muscular and cerebral dystrophy and muscle eye brain disease with bilateral multicystic leukodystrophy. MDDGA DOID:0111229 Orphanet:352687 lissencephaly type 2 with muscular and ocular involvement muscular dystrophy-dystroglycanopathy