{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=12280&ordering=name","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=12240&ordering=name","results":[{"accession":"CLO:0025172","name":"GM00050 cell","definition":"[' METHYLMALONICACIDURIA DUE TO METHYLMALONIC COA MUTASE DEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0025176","name":"GM00053 cell","definition":"[' GALACTOSEMIA']","term_type":"cell line"},{"accession":"CLO:0025177","name":"GM00054 cell","definition":"[' GALACTOSEMIA']","term_type":"cell line"},{"accession":"CLO:0025178","name":"GM00056 cell","definition":"[' PROPIONIC ACIDEMIA']","term_type":"cell line"},{"accession":"CLO:0025161","name":"GM00057 cell","definition":"[' PROPIONIC ACIDEMIA']","term_type":"cell line"},{"accession":"CLO:0025162","name":"GM00059 cell","definition":"[' HEXOSAMINIDASE A; HEXA CANAVAN DISEASE ASPARTOACYLASE; ASPA']","term_type":"cell line"},{"accession":"CLO:0025159","name":"GM00060 cell","definition":"[' CANAVAN DISEASE ASPARTOACYLASE; ASPA']","term_type":"cell line"},{"accession":"CLO:0025160","name":"GM00068 cell","definition":"[' LESCH-NYHAN SYNDROME; LNS']","term_type":"cell line"},{"accession":"CLO:0025165","name":"GM00071 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0025166","name":"GM00072 cell","definition":"[' WOLF-HIRSCHHORN SYNDROME; WHS CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0025163","name":"GM00073 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0025164","name":"GM00074 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0025167","name":"GM00077 cell","definition":"[' TAY-SACHS DISEASE; TSD HEXOSAMINIDASE A; HEXA']","term_type":"cell line"},{"accession":"CLO:0025168","name":"GM00078 cell","definition":"[' METACHROMATIC LEUKODYSTROPHY, LATE-INFANTILE']","term_type":"cell line"},{"accession":"CLO:0025149","name":"GM00080 cell","definition":"[' MUCOLIPIDOSIS II; ML2; ML II N-ACETYLGLUCOSAMINE-1-PHOSPHOTRANSFERASE, ALPHA/BETA SUBUNITS; GNPTAB']","term_type":"cell line"},{"accession":"CLO:0025150","name":"GM00081 cell","definition":"[' MUCOLIPIDOSIS II; ML2; ML II N-ACETYLGLUCOSAMINE-1-PHOSPHOTRANSFERASE, ALPHA/BETA SUBUNITS; GNPTAB']","term_type":"cell line"},{"accession":"CLO:0025151","name":"GM00082 cell","definition":"[' XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES']","term_type":"cell line"},{"accession":"CLO:0025152","name":"GM00083 cell","definition":"[' XY FEMALE - 306100 OR 233420']","term_type":"cell line"},{"accession":"CLO:0025153","name":"GM00084 cell","definition":"[' ANEUPLOID CHROMOSOME NUMBER - TRISOMY']","term_type":"cell line"},{"accession":"CLO:0025154","name":"GM00085 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"}]}