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All terms in MONDO

Label Id Description
inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3 MONDO_0014179
inclusion body myopathy with Paget disease of bone and frontotemporal dementia MONDO_0000507
twin reversal arterial perfusion syndrome MONDO_0041755
twin to twin transfusion syndrome MONDO_0019805
renal-hepatic-pancreatic dysplasia 2 MONDO_0014174
microcephaly 11, primary, autosomal recessive MONDO_0014173
spermatogenic failure 12 MONDO_0014172
complex cortical dysplasia with other brain malformations 4 MONDO_0014171
inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2 MONDO_0014178
myopia 22, autosomal dominant MONDO_0014177
myopia MONDO_0001384
hypotonia, infantile, with psychomotor retardation and characteristic facies MONDO_0014176
mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive MONDO_0014175
complex cortical dysplasia with other brain malformations 3 MONDO_0014170
obsolete genetic urticaria MONDO_0026141
perinatal intestinal perforation MONDO_0002196
intestinal perforation MONDO_0006807
minor vestibular glands adenoma MONDO_0002197
benign urethral neoplasm MONDO_0004177
vestibular gland benign neoplasm MONDO_0000626