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All terms in MONDO

Label Id Description
lipodystrophy MONDO_0006573
lichen nitidus MONDO_0006571
miliaria MONDO_0006580
X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome MONDO_0018569
obsolete COG2-CDG MONDO_0018568
non-syndromic renal or urinary tract malformation MONDO_0019720
3p25.3 microdeletion syndrome MONDO_0018564
partial deletion of the short arm of chromosome 3 MONDO_0016885
autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation MONDO_0018567
hereditary motor and sensory neuropathy, Okinawa type MONDO_0011468
Charcot-Marie-Tooth disease type 2 MONDO_0018993
short stature-advanced bone age-early-onset osteoarthritis syndrome MONDO_0018566
aggrecan-related bone disorder MONDO_0018239
precocious puberty in female MONDO_0018561
precocious puberty MONDO_0000088
anomaly of puberty or/and menstrual cycle MONDO_0015860
obsolete anterior urethral valve MONDO_0018560
adactyly of foot MONDO_0018563
non-syndromic terminal limb defects MONDO_0017421
genetic otorhinolaryngological malformation MONDO_0018562