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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
cystic fibrosis
MONDO_0009061
scapuloperoneal spinal muscular atrophy, autosomal recessive
MONDO_0010058
cystic disease of lung
MONDO_0009060
spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome
MONDO_0010051
obsolete spastic pseudosclerosis
MONDO_0010050
hereditary spherocytosis type 3
MONDO_0010053
spermatogenic failure 4
MONDO_0010052
bowenoid papulosis
MONDO_0022022
human papilloma virus infection
MONDO_0005161
Philadelphia-positive myelogenous leukemia
MONDO_0024685
tenosynovial giant cell tumor, diffuse type
MONDO_0024686
boylan dew greco syndrome
MONDO_0022025
congenital lactic acidosis, Saguenay-Lac-Saint-Jean type
MONDO_0009069
Boudhina Yedes Khiari syndrome
MONDO_0022020
cystinuria
MONDO_0009067
deafness, congenital, and familial myoclonic epilepsy
MONDO_0009077
familial isolated congenital asplenia
MONDO_0010066
autosomal recessive nonsyndromic hearing loss 1A
MONDO_0009076
spinocerebellar degeneration with slow eye movements
MONDO_0010065
Dandy-Walker malformation-postaxial polydactyly syndrome
MONDO_0009075