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All terms in MONDO

Label Id Description
spermatogenic failure 13 MONDO_0014365
mitochondrial complex III deficiency nuclear type 8 MONDO_0014364
autosomal recessive nonsyndromic hearing loss 101 MONDO_0014363
chromosome 16 inversion, 0.45-Mb MONDO_0014362
liver angiosarcoma MONDO_0002387
intracystic papillary adenoma MONDO_0002388
obsolete adenofibroma MONDO_0002389
Pacinian tumor MONDO_0002383
obsolete transitional cell carcinoma MONDO_0002384
benign cystic nephroma MONDO_0002385
mixed epithelial stromal tumor of the kidney MONDO_0002386
mixed epithelial stromal tumor MONDO_0003272
benign mesenchymoma MONDO_0002382
ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder MONDO_0014379
primary ciliary dyskinesia 29 MONDO_0014378
developmental and epileptic encephalopathy, 24 MONDO_0014377
cone-rod dystrophy 19 MONDO_0014372
developmental and epileptic encephalopathy, 23 MONDO_0014371
pontocerebellar hypoplasia type 2E MONDO_0014370
fibrosis of bile duct MONDO_0041959