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All terms in MONDO

Label Id Description
Chilton-Okur-Chung neurodevelopmental syndrome MONDO_0859239
fetal lung interstitial tumor MONDO_0017289
Xp22.13p22.2 duplication syndrome MONDO_0017284
auditory neuropathy, autosomal dominant 3 MONDO_0859235
penoscrotal transposition MONDO_0017285
neurodevelopmental disorder with neuromuscular and skeletal abnormalities MONDO_0859236
tempi syndrome MONDO_0017286
3-methylglutaconic aciduria, type VIIA MONDO_0859237
renal caliceal diverticuli-deafness syndrome MONDO_0017281
neurodevelopmental disorder with central hypotonia and dysmorphic facies MONDO_0859232
alveolar echinococcosis MONDO_0017282
DeSanto-Shinawi Syndrome due to 10p11.21p12.31 microdeletion MONDO_0017283
agammaglobulinemia 8b, autosomal recessive MONDO_0859234
spermatogenic failure 43 MONDO_0032898
neutropenia, severe congenital, 8, autosomal dominant MONDO_0032899
Kury-Isidor syndrome MONDO_0859230
refractory cytopenia of childhood MONDO_0044874
childhood myelodysplastic syndrome MONDO_0044873
drug hypersensitivity syndrome MONDO_0044876
coronary microvascular disorder MONDO_0044875