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All terms in MONDO

Label Id Description
adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency MONDO_0014899
keratoconus 4 MONDO_0012236
keratoconus MONDO_0015486
nemaline myopathy 6 MONDO_0012237
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3 MONDO_0014898
autosomal recessive progressive external ophthalmoplegia MONDO_0016810
Okur-Chung neurodevelopmental syndrome MONDO_0014893
myopia 10 MONDO_0012230
Charcot-Marie-Tooth disease type 2A2 MONDO_0012231
micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome MONDO_0014892
hyperuricemic nephropathy, familial juvenile type 4 MONDO_0014891
familial juvenile hyperuricemic nephropathy MONDO_0000608
PERCHING syndrome MONDO_0014890
cold-induced sweating syndrome MONDO_0015526
restricted to specific location MONDO_0045042
asymptomatic dengue MONDO_0000259
dengue disease MONDO_0005502
obsolete intestinal botulism MONDO_0000258
acute diarrhea MONDO_0000257
myopia 9 MONDO_0012229