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All terms in MONDO

Label Id Description
syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome MONDO_0014069
mitochondrial complex III deficiency nuclear type 3 MONDO_0014064
mitochondrial complex III deficiency nuclear type 2 MONDO_0014063
mitochondrial DNA deletion syndrome with progressive myopathy MONDO_0014062
progressive external ophthalmoplegia with mitochondrial DNA deletions MONDO_0000090
Steel syndrome MONDO_0014061
cone-rod dystrophy 17 MONDO_0014068
short ulna-dysmorphism-hypotonia-intellectual disability syndrome MONDO_0014067
mitochondrial complex III deficiency nuclear type 5 MONDO_0014066
mitochondrial complex III deficiency nuclear type 4 MONDO_0014065
progressive retinal dystrophy due to retinol transport defect MONDO_0014060
clear cell acanthoma MONDO_0002086
acanthoma MONDO_0002093
partial retinal vein occlusion MONDO_0002088
retinal vein occlusion MONDO_0006951
retinal vascular occlusion MONDO_0002089
vascular occlusion disorder MONDO_0020672
Richter syndrome MONDO_0002083
secondary neoplasm MONDO_0024882
B-cell chronic lymphocytic leukemia MONDO_0004948