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All terms in MONDO

Label Id Description
obsolete Heimler syndrome 2 MONDO_0014709
ring chromosome 14 MONDO_0014708
obsolete hereditary spherocytosis type 2 MONDO_0014721
autosomal dominant optic atrophy plus syndrome MONDO_0014720
autosomal dominant hereditary axonal motor and sensory neuropathy MONDO_0015360
spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome MONDO_0014725
Joubert syndrome 24 MONDO_0014724
PMP22-RAI1 contiguous gene duplication syndrome MONDO_0014723
Roifman syndrome MONDO_0014722
ampulla of vater mucinous adenocarcinoma MONDO_0002736
acute sanguinous otitis media MONDO_0002737
acute transudative otitis media MONDO_0002738
non-suppurative otitis media MONDO_0001212
obsolete prostate colloid adenocarcinoma MONDO_0002743
fallopian tube mucinous adenocarcinoma MONDO_0002744
fallopian tube mucinous tumor MONDO_0002745
uterine ligament mucinous adenocarcinoma MONDO_0002740
uterine ligament adenocarcinoma MONDO_0002741
developmental and epileptic encephalopathy, 34 MONDO_0014718
early-onset Lafora body disease MONDO_0014717