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| created at |
2025-11-26 04:53:50 UTC |
| updated at |
2025-11-27 01:00:35 UTC |
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Mondo ID - Mondo Label
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30,114 entries
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There is 0 pattern entry.
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camptodactyly-arthropathy-coxa vara-pericarditis syndrome
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0008828 |
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Athrombia, essential
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0008844 |
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3-methylcrotonyl-CoA carboxylase 1 deficiency
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0008861 |
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biliary malformation with renal tubular insufficiency
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0008868 |
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microcephalic osteodysplastic primordial dwarfism, type 3
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0008873 |
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cardiomyopathy associated with myopathy and sudden death
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0008916 |
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cholestasis with gallstone, ataxia, and visual disturbance
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0008968 |
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ciliary dyskinesia with transposition of ciliary microtubules
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0008985 |
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craniosynostosis with anomalies of the cranial base and digits
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0009037 |
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craniosynostosis-intellectual disability syndrome of 51N and Gettig
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0009040 |
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cutis marmorata telangiectatica congenita
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0009055 |
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endocardial fibroelastosis and coarctation of abdominal aorta
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0009170 |
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endothelial dystrophy, congenital hereditary, with nail hypoplasia
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0009171 |
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epiphyseal dysplasia of femoral head, myopia, and deafness
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0009190 |
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focal epithelial hyperplasia
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0009237 |
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