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All terms in MONDO

Label Id Description
46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency MONDO_0009923
Pseudouridinuria and mental defect MONDO_0009922
holoprosencephaly-postaxial polydactyly syndrome MONDO_0009921
Acrootoocular syndrome MONDO_0009920
HEC syndrome MONDO_0010901
intrauterine growth retardation with increased mitomycin c sensitivity MONDO_0010900
craniosynostosis, Adelaide type MONDO_0010903
spondyloepiphyseal dysplasia, Reardon type MONDO_0010902
cone-rod dystrophy 1 MONDO_0010905
setting-Sun phenomenon, familial benign MONDO_0010904
cutaneous sclerosis MONDO_0022907
cutis gyratum acanthosis nigricans craniosynostosis MONDO_0022908
cutis laxa osteoporosis MONDO_0022909
athyreotic congenital hypothyroidism MONDO_0022900
Crohn disease of the esophagus MONDO_0022901
cryoglobulinemia MONDO_0005576
epilepsy, idiopathic generalized, susceptibility to, 1 MONDO_0010918
chondrocalcinosis 1 MONDO_0010917
chondrocalcinosis MONDO_0001314
pulmonic stenosis and congenital nephrosis MONDO_0009939