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All terms in MONDO

Label Id Description
non-syndromic intestinal malformation MONDO_0015211
microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome MONDO_0014096
dilated cardiomyopathy 1JJ MONDO_0014095
severe congenital hypochromic anemia with ringed sideroblasts MONDO_0014094
nephrotic syndrome, type 8 MONDO_0014099
familial idiopathic steroid-resistant nephrotic syndrome MONDO_0019006
CIDEC-related familial partial lipodystrophy MONDO_0014098
familial partial lipodystrophy MONDO_0020088
retinitis pigmentosa 66 MONDO_0014093
schizophrenia 18 MONDO_0014092
schizophrenia, susceptibility to MONDO_0100182
mitochondrial complex V (ATP synthase) deficiency nuclear type 4 MONDO_0014091
combined oxidative phosphorylation deficiency 22 MONDO_0020727
polydactyly, postaxial, type A6 MONDO_0014090
postaxial polydactyly type A MONDO_0019673
acute myeloid leukemia, der12p MONDO_0100390
acute myeloid leukemia, t(2;12) MONDO_0100391
acute myeloid leukemia, t(11;17) MONDO_0100392
acute myeloid leukemia, t(8;16) MONDO_0100393
acute myeloid leukemia, t(1;22) MONDO_0100394