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All terms in MONDO

Label Id Description
polyglucosan body myopathy type 2 MONDO_0014526
combined oxidative phosphorylation defect type 23 MONDO_0014525
intellectual disability, autosomal recessive 47 MONDO_0014524
obsolete progressive muscular atrophy MONDO_0002538
obsolete oligodendroglioma MONDO_0002539
schwannoma MONDO_0002546
cellular schwannoma MONDO_0002548
spinal cord oligodendroglioma MONDO_0002541
adult oligodendroglioma MONDO_0002543
brain oligodendroglioma MONDO_0002544
chronic mountain sickness, susceptibility to MONDO_0014519
platelet-type bleeding disorder 19 MONDO_0014518
generalized epilepsy with febrile seizures plus, type 9 MONDO_0014517
childhood oligodendroglioma MONDO_0002540
lissencephaly 6 with microcephaly MONDO_0014534
microlissencephaly MONDO_0015204
developmental and epileptic encephalopathy, 28 MONDO_0014533
autosomal dominant mitochondrial myopathy with exercise intolerance MONDO_0014532
amyotrophic lateral sclerosis type 22 MONDO_0014531
fibrosis of extraocular muscles, congenital, 5 MONDO_0014538