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All terms in MONDO

Label Id Description
primary acquired red cell aplasia MONDO_0020113
vitamin D-dependent rickets, type 2A MONDO_0010186
vitamin D-dependent rickets, type 2 MONDO_0019642
ermine phenotype MONDO_0009196
vitiligo, progressive, with intellectual disability and urethral duplication MONDO_0010189
erythema of acral regions MONDO_0009195
familial isolated deficiency of vitamin E MONDO_0010188
immunodeficiency 32B MONDO_0009194
idiopathic gastroparesis MONDO_0034150
epithelial squamous dysplasia, keratinizing desquamative, of urinary tract MONDO_0009193
Wolcott-Rallison syndrome MONDO_0009192
Lowry-Wood syndrome MONDO_0009191
epiphyseal dysplasia of femoral head, myopia, and deafness MONDO_0009190
oculogastrointestinal muscular dystrophy MONDO_0010181
disorder of fucoglycosan synthesis MONDO_0017747
methylmalonic aciduria and homocystinuria type cblF MONDO_0010183
hypercarotenemia and vitamin A deficiency, autosomal recessive MONDO_0010182
hereditary hypercarotenemia and vitamin A deficiency MONDO_0007272
methylmalonic aciduria and homocystinuria type cblD MONDO_0010185
methylmalonic aciduria and homocystinuria type cblC MONDO_0010184