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All terms in MONDO

Label Id Description
hearing loss, autosomal dominant 85 MONDO_0859366
spinocerebellar ataxia, autosomal recessive 33 MONDO_0859360
cerebellar atrophy with seizures and variable developmental delay MONDO_0032788
neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia MONDO_0859361
intellectual developmental disorder, autosomal recessive 71 MONDO_0032789
hyperinsulinemic hypoglycemia, familial, 8 MONDO_0859362
autosomal recessive epidermolytic ichthyosis MONDO_0044742
orofacial cleft 8 MONDO_0029145
extraoral halitosis due to methanethiol oxidase deficiency MONDO_0029144
intellectual developmental disorder with hypertelorism and distinctive facies MONDO_0029143
hearing loss, autosomal recessive 111 MONDO_0029142
acute hypotension MONDO_0005174
hypotensive disorder MONDO_0005468
spermatogenic failure 34 MONDO_0029148
actinic keratosis MONDO_0005173
malignant epithelial tumor of salivary glands MONDO_0017167
benign insulitis MONDO_0005176
spermatogenic failure 33 MONDO_0029147
obsolete Saul-Wilson syndrome MONDO_0029146
aggressive insulitis MONDO_0005175