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All terms in MONDO

Label Id Description
autosomal recessive nonsyndromic hearing loss 1B MONDO_0012977
FG syndrome 4 MONDO_0010318
hemosiderosis, pulmonary, with deficiency of gamma-a globulin MONDO_0009336
primary ciliary dyskinesia 11 MONDO_0012978
intellectual disability, X-linked, with or without seizures, arx-related MONDO_0010317
hemolytic uremic syndrome, atypical, susceptibility to, 1 MONDO_0009335
hemolytic anemia with thermal sensitivity of red cells MONDO_0009334
hereditary elliptocytosis MONDO_0017319
syndromic X-linked intellectual disability Hedera type MONDO_0010319
mullerian derivatives-lymphangiectasia-polydactyly syndrome MONDO_0009333
isolated hemihyperplasia MONDO_0009331
dyschromatosis universalis hereditaria 2 MONDO_0012993
obsolete primary ciliary dyskinesia-retinitis pigmentosa syndrome MONDO_0010330
non-spherocytic hemolytic anemia due to hexokinase deficiency MONDO_0009340
dopa-responsive dystonia due to sepiapterin reductase deficiency MONDO_0012994
Kahrizi syndrome MONDO_0012991
X-linked intellectual disability-cubitus valgus-dysmorphism syndrome MONDO_0010332
pancreatic insufficiency-anemia-hyperostosis syndrome MONDO_0012992
exocrine pancreatic insufficiency MONDO_0001684
cytochrome-c oxidase deficiency disease MONDO_0009068