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All terms in MONDO

Label Id Description
candidemia MONDO_0044070
cardio-renal syndrome MONDO_0044079
myopathy, centronuclear, 2 MONDO_0009709
myopathy, myosin storage, autosomal recessive MONDO_0009708
myopathy with giant abnormal mitochondria MONDO_0009707
hereditary myopathy with lactic acidosis due to ISCU deficiency MONDO_0009706
carnitine palmitoyl transferase 1A deficiency MONDO_0009705
carnitine palmitoyl transferase II deficiency, myopathic form MONDO_0009704
myopathy with abnormal lipid metabolism MONDO_0009703
myopathy due to malate-aspartate shuttle defect MONDO_0009702
myopathy, granulovacuolar lobular, with electrical myotonia MONDO_0009701
obsolete Carey-Fineman-Ziter syndrome MONDO_0009700
familial atrial myxoma MONDO_0009719
myxedema MONDO_0009718
Richieri Costa-da Silva syndrome MONDO_0009716
myotonia congenita, autosomal recessive MONDO_0009715
Thomsen and Becker disease MONDO_0009710
myosclerosis MONDO_0009714
myopia 18, autosomal recessive MONDO_0009713
congenital multicore myopathy with external ophthalmoplegia MONDO_0009712