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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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PFAPA syndrome
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0018540 |
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PGM1-CDG
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0013968 |
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PGM3-CDG
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0014353 |
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PHACE syndrome
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0011676 |
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PHARC syndrome
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0012984 |
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PHAVER syndrome
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0009859 |
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PHGDH deficiency
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0011152 |
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PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome
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0035133 |
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PLA2G6-associated neurodegeneration
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0017998 |
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PLIN1-related familial partial lipodystrophy
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0013478 |
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PMM2-CDG
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0008907 |
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PMP22-RAI1 contiguous gene duplication syndrome
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0014723 |
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POEMS syndrome
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0017364 |
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PPARG-related familial partial lipodystrophy
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0011448 |
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PPoma
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0019957 |
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