autosomal recessive limb-girdle muscular dystrophy ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Limb-Girdle Muscular Dystrophy, Recessive ClinVar autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by OMIM:613158 ClinVar PMID:17878207 autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 ClinVar PMID:17576681 more ... autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 ClinVar PMID:17878207 more ... autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 ClinVar PMID:17878207 more ... autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 ClinVar PMID:18513969 more ... autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 ClinVar PMID:25741868 , PMID:28492532 autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 ClinVar PMID:26467025 , PMID:28492532 autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 ClinVar PMID:28492532 autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 ClinVar PMID:24033266 more ... autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 ClinVar PMID:25741868 more ... autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy limb-girdle more ... ClinVar PMID:25741868 autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 ClinVar PMID:25741868 more ... autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by OMIM:613158 ClinVar autosomal recessive limb-girdle muscular dystrophy type 2N ISO RGD:1313480 8554872 ClinVar Annotator: match by OMIM:613158 ClinVar PMID:18414213 congenital muscular dystrophy ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy ClinVar congenital muscular dystrophy-dystroglycanopathy type A1 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies more ... ClinVar PMID:25741868 , PMID:28492532 congenital muscular dystrophy-dystroglycanopathy type A1 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies more ... ClinVar PMID:17559086 more ... congenital muscular dystrophy-dystroglycanopathy type A1 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies more ... ClinVar PMID:25741868 more ... congenital muscular dystrophy-dystroglycanopathy type A1 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies more ... ClinVar PMID:17634419 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED ClinVar PMID:25741868 , PMID:28492532 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:17878207 , PMID:28492532 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:17576681 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:17576681 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:25741868 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:17878207 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:18513969 , PMID:28492532 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:22323514 , PMID:28492532 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:28492532 , PMID:29382405 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:17878207 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:17634419 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:15894594 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED ClinVar PMID:25741868 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:15894594 , PMID:28492532 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:25741868 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:17559086 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:28492532 , PMID:29175898 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:17878207 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:17634419 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:22958903 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:25267602 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:18414213 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:25741868 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by OMIM:613150 ClinVar congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 ClinVar PMID:15894594 more ... congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED ClinVar PMID:26467025 , PMID:28492532 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED ClinVar PMID:28492532 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by OMIM:613150 ClinVar PMID:15894594 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by OMIM:613150 ClinVar PMID:17878207 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by OMIM:613150 ClinVar PMID:16701995 , PMID:19299310 congenital muscular dystrophy-dystroglycanopathy type A2 ISO RGD:1313480 8554872 ClinVar Annotator: match by OMIM:613150 ClinVar PMID:19138766 hereditary sensory and autonomic neuropathy type 1C ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Hereditary sensory and autonomic neuropathy type IC ClinVar PMID:28492532 intellectual disability ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Intellectual disability ClinVar PMID:17878207 more ... intellectual disability ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Intellectual disability ClinVar PMID:25741868 more ... muscular dystrophy ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Muscular dystrophy ClinVar PMID:25741868 muscular dystrophy ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Muscular dystrophy ClinVar PMID:17634419 more ... Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 ClinVar PMID:17634419 more ... Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY more ... ClinVar PMID:25741868 Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 2 ISO RGD:1313480 8554872 ClinVar Annotator: match by term: MUSCULAR DYSTROPHY more ... ClinVar PMID:17634419 more ... Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 2 ISO RGD:1313480 8554872 ClinVar Annotator: match by OMIM:613156 ClinVar PMID:19138766 Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 2 ISO RGD:1313480 8554872 ClinVar Annotator: match by OMIM:613156 ClinVar PMID:16701995 , PMID:19299310 Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 2 ISO RGD:1313480 8554872 ClinVar Annotator: match by OMIM:613156 ClinVar PMID:17634419 Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 2 ISO RGD:1313480 8554872 ClinVar Annotator: match by OMIM:613156 ClinVar PMID:19299310