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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
achromatopsia 5
MONDO_0800196
cone dystrophy
MONDO_0000455
achromatopsia 6
MONDO_0800197
achalasia-alacrima syndrome
MONDO_0800195
immunodeficiency 83, susceptibility to viral infections
MONDO_0800187
encephalitis, acute, infection-induced, susceptibility to
MONDO_0800174
malignant hyperthermia, susceptibility to
MONDO_0800188
TEK-related primary glaucoma
MONDO_0800182
primary hereditary glaucoma
MONDO_0015485
CPOX-related hereditary coproporphyria
MONDO_0800180
PAX6-related ocular dysgenesis
MONDO_0800183
acute epiglottitis
MONDO_0041366
epiglottitis
MONDO_0005753
inborn disorder of ornithine, proline and hydroxyproline metabolism
MONDO_0800156
inborn disorder of lysine, hydroxylysine, and tryptophan metabolism
MONDO_0800157
inborn disorder of tryptophan metabolism
MONDO_0017350
inborn disorder of the metabolism of sulfur-containing amino acids and hydrogen sulfide
MONDO_0800154
inborn disorder of glycine and serine metabolism
MONDO_0800155
glycine metabolism disease
MONDO_0045020
inborn disorder of serine family metabolism
MONDO_0019239