{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=13460&ordering=-accession","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=13420&ordering=-accession","results":[{"accession":"CLO:0029568","name":"GM00930 cell","definition":"[' METHYLMALONICACIDURIA DUE TO METHYLMALONIC COA MUTASE DEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0029567","name":"GM00931 cell","definition":"[' PORPHYRIA, ACUTE INTERMITTENT']","term_type":"cell line"},{"accession":"CLO:0029566","name":"GM20399 cell","definition":"[' ALPERS DIFFUSE DEGENERATION OF CEREBRAL GRAY MATTER WITH HEPATIC CIRRHOSIS POLYMERASE, DNA, GAMMA; POLG']","term_type":"cell line"},{"accession":"CLO:0029565","name":"GM00922 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0029564","name":"GM00919 cell","definition":"[' HOMOCYSTINURIA']","term_type":"cell line"},{"accession":"CLO:0029563","name":"GM00918 cell","definition":"[' GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I']","term_type":"cell line"},{"accession":"CLO:0029562","name":"GM00914 cell","definition":"[' RETINOBLASTOMA, SPORADIC']","term_type":"cell line"},{"accession":"CLO:0029561","name":"GM00911 cell","definition":"[' METHIONINE ADENOSYLTRANSFERASE DEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0029560","name":"GM00910 cell","definition":"[' CYSTINOSIS, NEPHROPATHIC; CTNS']","term_type":"cell line"},{"accession":"CLO:0029559","name":"GM20378 cell","definition":"[' CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 CLN2 GENE; CLN2']","term_type":"cell line"},{"accession":"CLO:0029558","name":"GM20379 cell","definition":"[' CEROID LIPOFUSCINOSIS, NEURONAL 1, INFANTILE; CLN1 PALMITOYL-PROTEIN THIOESTERASE 1; PPT1']","term_type":"cell line"},{"accession":"CLO:0029557","name":"GM20380 cell","definition":"[' CEROID LIPOFUSCINOSIS, NEURONAL 1, INFANTILE; CLN1 PALMITOYL-PROTEIN THIOESTERASE 1; PPT1']","term_type":"cell line"},{"accession":"CLO:0029556","name":"GM20381 cell","definition":"[' CEROID LIPOFUSCINOSIS, NEURONAL 3, JUVENILE; CLN3 CLN3 GENE; CLN3']","term_type":"cell line"},{"accession":"CLO:0029555","name":"GM20382 cell","definition":"[' CEROID LIPOFUSCINOSIS, NEURONAL 3, JUVENILE; CLN3 CLN3 GENE; CLN3']","term_type":"cell line"},{"accession":"CLO:0029554","name":"GM20383 cell","definition":"[' CEROID LIPOFUSCINOSIS, NEURONAL 3, JUVENILE; CLN3 CLN3 GENE; CLN3']","term_type":"cell line"},{"accession":"CLO:0029553","name":"GM20384 cell","definition":"[' CEROID LIPOFUSCINOSIS, NEURONAL 3, JUVENILE; CLN3 CLN3 GENE; CLN3']","term_type":"cell line"},{"accession":"CLO:0029552","name":"GM00942 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE MUCOPOLYSACCHARIDOSIS TYPE VI']","term_type":"cell line"},{"accession":"CLO:0029551","name":"GM20385 cell","definition":"[' CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 CLN2 GENE; CLN2']","term_type":"cell line"},{"accession":"CLO:0029550","name":"GM00943 cell","definition":"[' MUCOPOLYSACCHARIDOSIS TYPE VI']","term_type":"cell line"},{"accession":"CLO:0029549","name":"GM00945 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"}]}