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All terms in MONDO

Label Id Description
combined oxidative phosphorylation defect type 17 MONDO_0014190
obsolete genetic neuromuscular disease MONDO_0026167
obsolete genetic immune deficiency with skin involvement MONDO_0026166
obsolete genetic glomerular disease MONDO_0026192
obsolete genetic thrombotic microangiopathy MONDO_0026193
obsolete genetic malformation syndrome with odontal and/or periodontal component MONDO_0026190
obsolete genetic renal or urinary tract malformation MONDO_0026181
obsolete genetic cranial malformation MONDO_0026182
obsolete genetic congenital limb malformation MONDO_0026180
obsolete genetic respiratory or mediastinal malformation MONDO_0026185
obsolete genetic developmental defect of the eye MONDO_0026186
obsolete genetic digestive tract malformation MONDO_0026183
obsolete genetic visceral malformation of the liver, biliary tract, pancreas or spleen MONDO_0026184
obsolete genetic branchial arch or oral-acral syndrome MONDO_0026189
obsolete genetic malformation syndrome with short stature MONDO_0026187
obsolete genetic overgrowth/obesity syndrome MONDO_0026188
breasts and/or nipples, aplasia or hypoplasia of, 1 MONDO_0100490
isolated congenital breast hypoplasia/aplasia MONDO_0015855
generalized pustular psoriasis MONDO_0100491
pustular psoriasis MONDO_0022205