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All terms in MONDO

Label Id Description
craniostenosis cataract MONDO_0022888
inborn disorder of phenylalanine and tyrosine metabolism MONDO_0019235
craniostenosis with congenital heart disease intellectual disability MONDO_0022889
pyrimidine metabolism disease MONDO_0037937
craniosynostosis Maroteaux Fonfria type MONDO_0022891
craniosynostosis alopecia brain defect MONDO_0022892
craniosynostosis arthrogryposis cleft palate MONDO_0022893
inborn disorder of ornithine or proline metabolism MONDO_0019230
craniosynostosis autosomal dominant MONDO_0022894
craniosynostosis cleft lip palate arthrogryposis MONDO_0022895
craniosynostosis contractures cleft MONDO_0022896
craniosynostosis exostoses nevus epibulbar dermoid MONDO_0022897
craniosynostosis intellectual disability heart defects MONDO_0022898
autosomal dominant nocturnal frontal lobe epilepsy 1 MONDO_0010899
canine teeth, absence of upper permanent MONDO_0007258
obsolete lens position anomaly MONDO_0020236
craniofaciofrontodigital syndrome MONDO_0007259
lens size anomaly MONDO_0020235
obsolete craniofacial anomaly with cataract MONDO_0020234
Shwachman-Diamond syndrome 2 MONDO_0044205