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All terms in MONDO

Label Id Description
hearing loss, autosomal dominant 89 MONDO_0859528
oocyte maturation defect 14 MONDO_0859521
obsolete mitochondrial disease MONDO_0019055
spermatogenic failure 81 MONDO_0859522
obsolete neurometabolic disease MONDO_0019058
obsolete rare constitutional aplastic anemia MONDO_0019057
hearing loss, autosomal dominant 86 MONDO_0859524
obsolete partial autosomal trisomy/tetrasomy MONDO_0020052
obsolete lysosomal disease MONDO_0019051
obsolete total autosomal trisomy MONDO_0020051
obsolete autosomal trisomy MONDO_0020050
Mitochondrial complex IV deficiency, nuclear type 23 MONDO_0859520
obsolete gonosome number anomaly MONDO_0020059
obsolete uniparental disomy of paternal origin MONDO_0020057
obsolete uniparental disomy of maternal origin MONDO_0020056
pseudohypoparathyroidism type 1A MONDO_0007078
alcohol dependence MONDO_0007079
obsolete autosomal uniparental disomy MONDO_0020055
obsolete partial autosomal monosomy MONDO_0020054
obsolete ocular albinism with sensorineural deafness MONDO_0007076