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All terms in MONDO

Label Id Description
severe combined immunodeficiency due to LAT deficiency MONDO_0044721
familial progressive hyperpigmentation MONDO_0013648
pseudohypoaldosteronism type 2A MONDO_0007772
pseudohypoaldosteronism type 2 MONDO_0019162
hyperpigmentation of Fuldauer and Kuijpers MONDO_0007770
hypercalcemia, infantile, 1 MONDO_0020739
isolated partial cerebellar vermis agenesis MONDO_0017109
isolated cerebellar vermis agenesis MONDO_0017107
multiple benign circumferential skin creases on limbs 1 MONDO_0020738
pancreatic carcinoma with mixed differentiation MONDO_0044727
optic atrophy 10 with or without ataxia, intellectual disability, and seizures MONDO_0020737
uncombable hair syndrome 1 MONDO_0020736
ACTH-independent macronodular adrenal hyperplasia 1 MONDO_0020735
glioependymal/ependymal cyst MONDO_0017105
X-linked intellectual disability, Golabi-Ito-hall type MONDO_0019768
3-methylglutaconic aciduria type 9 MONDO_0044724
obsolete erythrocyte AMP deaminase deficiency MONDO_0020734
hamel cerebro-palato-cardiac syndrome MONDO_0019767
retrocerebellar cyst MONDO_0017106
3-methylglutaconic aciduria type 8 MONDO_0044723