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All terms in MONDO

Label Id Description
autosomal recessive severe congenital neutropenia due to CXCR2 deficiency MONDO_0018487
autosomal recessive severe congenital neutropenia MONDO_0028226
autoimmune encephalopathy with parasomnia and obstructive sleep apnea MONDO_0018489
sleep-wake disorder MONDO_0003406
autoimmune disorder of central nervous system MONDO_0000568
semicircular canal dehiscence syndrome MONDO_0018484
otorhinolaryngologic disease MONDO_0024623
secondary pulmonary alveolar proteinosis MONDO_0018483
pulmonary alveolar proteinosis MONDO_0001437
secondary interstitial lung disease in childhood and adulthood MONDO_0017034
visual snow syndrome MONDO_0018486
glycogen storage disease due to acid maltase deficiency, late-onset MONDO_0018485
glycogen storage disease II MONDO_0009290
carcinoma of esophagus, salivary gland type MONDO_0018480
carcinoma of esophagus MONDO_0019086
obsolete squamous cell carcinoma of stomach MONDO_0018482
undifferentiated carcinoma of esophagus MONDO_0018481
esophageal squamous cell carcinoma MONDO_0005580
double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy MONDO_0018499
double outlet right ventricle MONDO_0018089