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All terms in MONDO

Label Id Description
fatty acyl-CoA reductase defects MONDO_0100275
disorder of defective peroxisomal and mitochondrial fission MONDO_0100276
disorder of peroxisomal alpha oxidation MONDO_0100277
alanine glyoxylate aminotransferase deficiency MONDO_0100278
disorder of glyoxylate metabolism MONDO_0017703
peroxisome biogenesis disorder due to PEX11B defect MONDO_0100279
Waldenstrom macroglobulinemia MONDO_0100280
lymphoplasmacytic lymphoma MONDO_0000432
indolent B-cell non-Hodgkin lymphoma MONDO_0017594
macroglobulinemia, Waldenstrom, 1 MONDO_0100281
SC phocomelia syndrome MONDO_0100282
Roberts-SC phocomelia syndrome MONDO_0100253
overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes MONDO_0100283
X-linked intellectual disability MONDO_0100284
extrahepatic biliary atresia MONDO_0100285
respiratory syncytial virus bronchiolitis MONDO_0100286
bronchiolitis MONDO_0002465
respiratory syncytial virus infectious disease MONDO_0001577
POLE-related polyposis and colorectal cancer syndrome MONDO_0100287
familial colorectal cancer MONDO_0023113