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All terms in MONDO

Label Id Description
blepharonasofacial malformation syndrome MONDO_0007200
disorder of phenylalanine metabolism MONDO_0017306
phenformin 4-hydroxylation MONDO_0009860
palmoplantar keratoderma, Bothnian type MONDO_0010849
autosomal recessive nonsyndromic hearing loss 3 MONDO_0010860
type 1 diabetes mellitus 4 MONDO_0010862
type 1 diabetes mellitus 3 MONDO_0010861
type 1 diabetes mellitus 7 MONDO_0010864
type 1 diabetes mellitus 5 MONDO_0010863
congenital nonhemolytic jaundice MONDO_0022846
congenital stenosis of cervical medullary canal MONDO_0022849
obsolete congenital sucrose isomaltose malabsorption MONDO_0022850
Dennis-Fairhurst-Moore syndrome MONDO_0022851
brachydactyly type A4 MONDO_0007218
Osebold-Remondini syndrome MONDO_0007219
short stature due to growth hormone qualitative anomaly MONDO_0009879
brachydactyly type A2 MONDO_0007216
brachydactyly type A3 MONDO_0007217
pituitary hormone deficiency, combined, 2 MONDO_0009878
congenital unilateral pulmonary hypoplasia MONDO_0022854