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All terms in MONDO

Label Id Description
obsolete tumoral calcinosis MONDO_0000101
intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type MONDO_0026733
obsolete trichorhinophalangeal syndrome MONDO_0000100
Basilicata-Akhtar syndrome MONDO_0026730
obsolete protein C deficiency MONDO_0002767
hypothyroidism, congenital, nongoitrous, 8 MONDO_0026731
true hermaphroditism MONDO_0002768
cervical verrucous carcinoma MONDO_0002761
obsolete apnea MONDO_0000106
esophagus verrucous carcinoma MONDO_0002762
urethral verrucous carcinoma MONDO_0002763
urethra squamous cell carcinoma MONDO_0002764
obsolete Wilms tumor MONDO_0000103
autosomal recessive nonsyndromic hearing loss 97 MONDO_0014739
autosomal dominant nonsyndromic hearing loss 69 MONDO_0014738
dehydrated hereditary stomatocytosis 2 MONDO_0014737
primary coenzyme Q10 deficiency 8 MONDO_0014754
autosomal recessive optic atrophy MONDO_0014753
nephrotic syndrome, type 11 MONDO_0014752
palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome MONDO_0014751