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All terms in MONDO

Label Id Description
obsolete Pierre Robin syndrome associated with collagen disease MONDO_0024145
obsolete familial adenomatous polyposis MONDO_0000199
obsolete Pierre Robin syndrome associated with branchial archs anomalies MONDO_0024148
obsolete Pierre Robin syndrome associated with a chromosomal anomaly MONDO_0024147
obsolete linear skin defects with multiple congenital anomalies MONDO_0000198
obsolete Pierre Robin syndrome associated with bone disease MONDO_0024149
cortisone reductase deficiency MONDO_0000193
polyglucosan body myopathy MONDO_0000192
obsolete renal hypodysplasia/aplasia MONDO_0000191
obsolete singleton-Merten syndrome MONDO_0000197
obsolete ataxia-oculomotor apraxia MONDO_0000196
obsolete atrial standstill MONDO_0000195
obsolete Otofaciocervical syndrome MONDO_0000194
neuronal ceroid lipofuscinosis 9 MONDO_0012188
obsolete Amish infantile epilepsy syndrome MONDO_0012189
skeletal dysplasia, rhizomelic, with retinitis pigmentosa MONDO_0012182
melanoma, cutaneous malignant, susceptibility to, 3 MONDO_0012183
arrhythmogenic right ventricular dysplasia 9 MONDO_0012180
hereditary spastic paraplegia 27 MONDO_0012181
Fanconi anemia complementation group I MONDO_0012186