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| created at |
2021-12-13 15:49:09 UTC |
| updated at |
2021-12-13 16:09:58 UTC |
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Mondo Disease Ontology (Mondo).
Mondo aims to harmonizes disease definitions across the world. For more details on this ontology see:
Mondo website: https://monarch-initiative.github.io/mondo
OBO Foundry Mondo page: http://obofoundry.org/ontology/mondo.html
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24,745 entries
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There is 0 pattern entry.
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Prader-Willi syndrome due to imprinting mutation
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0015786 |
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Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
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0020298 |
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Prader-Willi syndrome due to paternal 15q11q13 deletion
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0020301 |
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Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
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0015783 |
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Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
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0015784 |
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Prader-Willi syndrome due to translocation
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0015785 |
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Prader-Willi-like syndrome
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0018354 |
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Prader-Willi-like syndrome due to point mutation
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0018355 |
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Prata-Liberal-Goncalves syndrome
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0017568 |
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Preaxial polydactyly of toes
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0017457 |
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Preaxial polydactyly of toes, bilateral
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0017538 |
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Preaxial polydactyly of toes, unilateral
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0017537 |
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Preeyasombat-Varavithya syndrome
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0060781 |
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Prepapillary vascular loops
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0009907 |
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Prieto syndrome
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0010667 |
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