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All terms in MONDO

Label Id Description
cataract-deafness-hypogonadism syndrome MONDO_0015325
cataract-intellectual disability-anal atresia-urinary defects syndrome MONDO_0015324
obsolete malformation syndrome with short stature MONDO_0015329
obsolete rare bone development disorder MONDO_0015328
multifocal atrial tachycardia MONDO_0017988
non-syndromic bicoronal and sagittal craniosynostosis MONDO_0850083
syngnathia-cleft palate syndrome MONDO_0017981
non-syndromic pansynostosis MONDO_0850084
obsolete humeroradial synostosis MONDO_0017982
humero-radio-ulnar synostosis MONDO_0017983
familial lambdoid synostosis MONDO_0017984
primary hypomagnesemia-generalized seizures-intellectual disability-obesity syndrome MONDO_0850087
obsolete Pierre Robin syndrome associated with bone disease MONDO_0015322
EGF-related primary hypomagnesemia with intellectual disability MONDO_0850088
obsolete Pierre Robin syndrome associated with branchial archs anomalies MONDO_0015321
Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation MONDO_0850089
obsolete Pierre Robin syndrome associated with a chromosomal anomaly MONDO_0015320
syngnathia multiple anomalies MONDO_0017980
intellectual developmental disorder, autosomal dominant 64 MONDO_0030934
conventional leiomyosarcoma MONDO_0003348