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All terms in MONDO

Label Id Description
asperger syndrome, susceptibility to, 1 MONDO_0012082
primary ciliary dyskinesia 4 MONDO_0012087
primary ciliary dyskinesia 5 MONDO_0012088
primary ciliary dyskinesia 3 MONDO_0012085
autosomal dominant nonsyndromic hearing loss 31 MONDO_0012086
neuronopathy, distal hereditary motor, type 2B MONDO_0012080
distal hereditary motor neuropathy type 2 MONDO_0015352
prostate cancer, hereditary, 4 MONDO_0012094
intellectual disability-brachydactyly-Pierre Robin syndrome MONDO_0012095
hereditary sensory and autonomic neuropathy type 5 MONDO_0012092
prostate cancer, hereditary, 3 MONDO_0012093
KAT6B-related multiple congenital anomalies syndrome MONDO_0036042
spinocerebellar ataxia type 20 MONDO_0012098
AICA-ribosiduria MONDO_0012099
euthyroid dysprealbuminemic hyperthyroxinemia MONDO_0036045
hyperthyroxinemia MONDO_0005333
Charcot-Marie-Tooth disease axonal type 2L MONDO_0012096
spondylocostal dysostosis 2, autosomal recessive MONDO_0012097
autosomal dominant nonsyndromic hearing loss 47 MONDO_0012090
autosomal recessive nonsyndromic hearing loss 32 MONDO_0012091