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All terms in MONDO

Label Id Description
upper aerodigestive tract neoplasm MONDO_0005398
venous thromboembolism MONDO_0005399
gout MONDO_0005393
celiac trunk compression syndrome MONDO_0017388
tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria MONDO_0017389
familial clubfoot due to PITX1 point mutation MONDO_0017383
acute generalized exanthematous pustulosis MONDO_0017384
myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive MONDO_0030341
microcephaly 28, primary, autosomal recessive MONDO_0030339
congenital herpes simplex virus infection MONDO_0017381
familial clubfoot due to 5q31 microdeletion MONDO_0017382
diarrhea 12, with microvillus atrophy MONDO_0030335
anencephaly 2 MONDO_0030338
cutis laxa, autosomal recessive, type 2E MONDO_0030337
obsolete disease of receptor activity MONDO_0044977
obsolete disease of catalytic activity MONDO_0044976
obsolete disease by cell type MONDO_0044979
obsolete disease of cell nucleus MONDO_0044978
Martsolf syndrome 2 MONDO_0030376
Martsolf syndrome MONDO_0023910