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All terms in MONDO

Label Id Description
congenital myopathy with reduced type 2 muscle fibers MONDO_0034109
isolated thyroid-stimulating hormone deficiency MONDO_0010139
Ehlers-Danlos syndrome, cardiac valvular type MONDO_0009159
Ehlers-Danlos syndrome, fibronectinemic type MONDO_0009158
split hand-foot malformation 6 MONDO_0009157
ectrodactyly-polydactyly syndrome MONDO_0009156
EEM syndrome MONDO_0009155
Aicardi-Goutieres syndrome 1 MONDO_0009165
trigonocephaly-bifid nose-acral anomalies syndrome MONDO_0010154
encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts MONDO_0009164
trichoodontoonychial dysplasia MONDO_0010153
encephalomalacia, multilocular MONDO_0009163
Troyer syndrome MONDO_0010156
Ellis-van Creveld syndrome MONDO_0009162
Dorfman-Chanarin disease MONDO_0010155
neutral lipid storage disease MONDO_0015611
Ehlers-Danlos syndrome, dermatosparaxis type MONDO_0009161
T-substance anomaly MONDO_0010158
obsolete Ehlers-Danlos syndrome, type 6 MONDO_0009160
Tryptophanuria with dwarfism MONDO_0010157