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All terms in MONDO

Label Id Description
Mauriac syndrome MONDO_0022435
severe X-linked mitochondrial encephalomyopathy MONDO_0010437
channelopathy-associated congenital insensitivity to pain, autosomal recessive MONDO_0009459
chromosome Xq28 duplication syndrome MONDO_0010436
syndromic X-linked intellectual disability Lubs type MONDO_0010283
Schimke immuno-osseous dysplasia MONDO_0009458
cardiomyopathy, fatal fetal, due to myocardial calcification MONDO_0010439
immunoglobulin d level in plasma, low MONDO_0009457
paroxysmal nocturnal hemoglobinuria 1 MONDO_0010438
Immunoerythromyeloid hypoplasia MONDO_0009456
reticular dysgenesis MONDO_0009973
immunodeficiency, partial combined, with absence of HLA Determinants and beta-2-microglobulin from lymphocytes MONDO_0009455
immunodeficiency-centromeric instability-facial anomalies syndrome 1 MONDO_0009454
immune deficiency disease MONDO_0009453
Vici syndrome MONDO_0009452
inosine phosphorylase deficiency, immune defect due to MONDO_0009462
intellectual disability, X-linked 41 MONDO_0010451
spermatogenic failure 5 MONDO_0009461
intellectual disability, X-linked 89 MONDO_0010450
indolylacroyl glycinuria with intellectual disability MONDO_0009460