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All terms in MONDO

Label Id Description
atypical Rett syndrome MONDO_0017746
syndromic X-linked intellectual disability 14 MONDO_0010398
severe neonatal-onset encephalopathy with microcephaly MONDO_0010397
chromosome Xp21 deletion syndrome MONDO_0010399
ocular albinism with late-onset sensorineural deafness MONDO_0010390
ocular albinism MONDO_0017304
glycogen storage disease due to phosphoglycerate kinase 1 deficiency MONDO_0010392
angioma serpiginosum, X-linked MONDO_0010391
angioma serpiginosum MONDO_0019803
obsolete leukoencephalopathy-metaphyseal chondrodysplasia syndrome MONDO_0010394
intellectual disability, X-linked 93 MONDO_0010393
retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene MONDO_0022397
aglossia and situs inversus MONDO_0022398
situs inversus MONDO_0010029
retinal ciliopathy due to mutation in the RPGR gene MONDO_0022399
acute lymphoblastic leukemia congenital sporadic aniridia MONDO_0022380
aniridia MONDO_0019172
hypervitaminosis a, susceptibility to MONDO_0009409
hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase MONDO_0009408
hypertrophic neuropathy and cataract MONDO_0009407