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All terms in MONDO

Label Id Description
osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome MONDO_0017196
combined oxidative phosphorylation deficiency 56 MONDO_0859323
osteopathia striata-pigmentary dermopathy-white forelock syndrome MONDO_0017197
developmental delay, language impairment, and ocular abnormalities MONDO_0859324
familial osteosclerosis MONDO_0042973
developmental and epileptic encephalopathy 109 MONDO_0859325
osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome MONDO_0017199
sporadic secreting paraganglioma MONDO_0017192
sporadic pheochromocytoma/secreting paraganglioma MONDO_0017190
symptomatic form of Coffin-Lowry syndrome in female carriers MONDO_0017193
mitochondrial complex I deficiency, nuclear type 39 MONDO_0859320
mitochondrial complex 3 deficiency, nuclear type 11 MONDO_0859321
sporadic pheochromocytoma MONDO_0017191
solid pseudopapillary neoplasm of the pancreas MONDO_0044786
desmoplastic melanoma MONDO_0044785
perihilar intrahepatic cholangiocarcinoma MONDO_0044788
nephrotic syndrome of childhood - steroid sensitive MONDO_0044781
myxoma MONDO_0044784
solid papillary breast carcinoma MONDO_0044783
breast papillary carcinoma MONDO_0003532