has material basis in germline mutation in SLC16A12 autosomal dominant disease juvenile cataract-microcornea-renal glucosuria syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/cataract_47 https://www.malacards.org/card/juvenile_cataract_microcornea_renal_glucosuria_syndrome CTRCT47 Juvenile cataract - microcornea - renal glucosuria is an extremely rare autosomal dominant association reported in a single Swiss family and characterized clinically by juvenile cataract associated with bilateral microcornea, and renal glucosuria without other renal tubular defects. MESH:C567434 UMLS:C4310806 SCTID:722457005 OMIM:612018 Orphanet:247794 MONDO:0012786 cataract, juvenile, with microcornea and glucosuria GARD:0017196 MEDGEN:934773 CJMG cataract 47, juvenile, with microcornea DOID:0070353 juvenile cataract-microcornea-renal glucosuria syndrome disorder of carbohydrate transmembrane transport and absorption obsolete nephropathy secondary to a storage or other metabolic disease