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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
penile cancer
MONDO_0001325
MAN1B1-congenital disorder of glycosylation
MONDO_0018349
obsolete polyglucosan body myopathy type 1
MONDO_0018348
obsolete T+ B+ severe combined immunodeficiency
MONDO_0018345
periodic paralysis with transient compartment-like syndrome
MONDO_0018344
periodic paralysis
MONDO_0016122
severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome
MONDO_0018347
triopia
MONDO_0031322
pupil disorder
MONDO_0002285
ferro-cerebro-cutaneous syndrome
MONDO_0018346
3q27.3 microdeletion syndrome
MONDO_0018341
syndrome caused by partial chromosomal deletion
MONDO_0000761
hereditary isolated aplastic anemia
MONDO_0018340
inherited aplastic anemia
MONDO_0001713
obsolete krt1-related diffuse nonepidermolytic keratoderma
MONDO_0033981
periodic paralysis with later-onset distal motor neuropathy
MONDO_0018343
familial periodic paralysis
MONDO_0000995
neuromuscular disease
MONDO_0019056
RELA fusion-positive ependymoma
MONDO_0033980
ependymal tumor
MONDO_0003266