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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
hypogonadism-mitral valve prolapse-intellectual disability syndrome
MONDO_0016385
acquired hypertrichosis lanuginosa
MONDO_0016380
hypertrichosis lanuginosa congenita
MONDO_0016381
autonomic dysreflexia
MONDO_0043975
obsolete lysosomal disease with epilepsy
MONDO_0016397
obsolete peroxisomal disease with epilepsy
MONDO_0016398
obsolete amino acid or protein metabolism disease with epilepsy
MONDO_0016399
hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome
MONDO_0016393
arhinia, choanal atresia, and microphthalmia
MONDO_0011323
sporadic infantile bilateral striatal necrosis
MONDO_0016394
infantile bilateral striatal necrosis
MONDO_0015518
foveal hypoplasia-presenile cataract syndrome
MONDO_0016395
pontocerebellar hypoplasia type 1
MONDO_0016396
genetic hypoparathyroidism
MONDO_0016165
cerebellar hypoplasia-tapetoretinal degeneration syndrome
MONDO_0016392
cubital tunnel syndrome
MONDO_0043982
ulnar neuropathy
MONDO_0007006
central nervous system lupus
MONDO_0043985
alopecia universalis
MONDO_0800198
Angelman syndrome chromosome region
MONDO_0800199