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| created at |
2024-09-23 15:44:32 UTC |
| updated at |
2024-11-28 14:07:45 UTC |
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Terms of phenotypic abnormality as defined in HP.
The entries were initially sourced from the HP version 2024-08-13 as stored in BioPortal.
Namespace: http://purl.obolibrary.org/obo/
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40,349 entries
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There is 0 pattern entry.
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Myasthenia
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HP:0003473 |
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Mydriasis
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HP:0011499 |
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Myelitis
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HP:0012486 |
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Myelocystocele
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HP:0030709 |
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Myelodysplasia
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HP:0002863 |
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Myelofibrosis
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HP:0011974 |
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Myelokathexis
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HP:0031160 |
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Myelomeningocele
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HP:0002475 |
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Myelopathy
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HP:0002196 |
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Myeloschisis
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HP:0030708 |
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Myocarditis
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HP:0012819 |
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Myoclonus
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HP:0001336 |
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Myodeopsia
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HP:0100832 |
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Myodesopsia
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HP:0100832 |
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Myofibromatosis
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HP:0020135 |
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