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Mondo Disease Ontology
MONDO
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Label
Id
Description
spastic paraplegia-Paget disease of bone syndrome
MONDO_0018005
autosomal dominant complex spastic paraplegia
MONDO_0015087
neurodevelopmental disorder with alopecia and brain abnormalities
MONDO_0033642
disorder of polyamine metabolism
MONDO_0800159
combined carcinoid and adenocarcinoma
MONDO_0021659
cleft palate, proliferative retinopathy, and developmental delay
MONDO_0033641
hereditary thrombocytosis with transverse limb defect
MONDO_0018000
inherited blood coagulation disorder
MONDO_0021181
congenital hematological disorder
MONDO_0009332
vitamin D-dependent rickets, type 3
MONDO_0033640
vitamin D-dependent rickets
MONDO_0024299
adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
MONDO_0018002
inverse Klippel-Trenaunay syndrome
MONDO_0018001
congenital vascular bone syndrome
MONDO_0016524
deep seated dermatophytosis
MONDO_0021660
tinea infection
MONDO_0005982
coronary atherosclerosis
MONDO_0021661
atherosclerosis
MONDO_0005311
biliary tract neoplasm
MONDO_0005304
mitochondrial complex 4 deficiency, nuclear type 10
MONDO_0033639