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All terms in MONDO

Label Id Description
deafness peripheral neuropathy arterial disease MONDO_0022945
deafness progressive cataract autosomal dominant MONDO_0022946
Deal Barratt Dillon syndrome MONDO_0022948
defective apolipoprotein b-100 MONDO_0022949
chondrocalcinosis 2 MONDO_0007319
obsolete rare disorder with entropion MONDO_0034926
obsolete chlorpropamide-alcohol flushing MONDO_0007317
retinal degeneration-nanophthalmos-glaucoma syndrome MONDO_0009978
obsolete inflammatory/autoimmune disorder involving the lacrimal system MONDO_0034923
Chiari malformation type I MONDO_0007316
obsolete Knobloch syndrome MONDO_0009977
delta-1-pyrroline-5-carboxylate dehydrogenase deficiency MONDO_0022953
Wiskott-Aldrich syndrome, autosomal dominant form MONDO_0010954
retinal degeneration and epilepsy MONDO_0009976
cheilitis glandularis MONDO_0007313
Fanconi anemia complementation group E MONDO_0010953
chemodectoma, intraabdominal, with cutaneous angiolipomas MONDO_0007314
enamel hypoplasia, cataracts, and aqueductal stenosis MONDO_0010956
familial hemophagocytic lymphohistiocytosis type 1 MONDO_0009974
Charcot-Marie-Tooth disease type 1E MONDO_0007311