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| created at |
2024-09-23 05:55:30 UTC |
| updated at |
2024-09-23 18:21:54 UTC |
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The OMIM entries, compiled in the following way.
1. The original entries were downloaded from BioPortal, on Sep. 23, 2024.
2. Only the original OMIM entries were extracted, which excluded the STY and MTHU entries.
Namespace for Semantic Web: http://purl.bioontology.org/ontology/OMIM/
Namespace for the OMIM web pages: https://www.omim.org/entry/
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116,330 entries
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There is 0 pattern entry.
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AME
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151385 |
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AML1
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151385 |
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CBFA2
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151385 |
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PEBP2-ALPHA-B
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151385 |
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PEBP2AB
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151385 |
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TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME
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151385 |
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RUNX1
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151385 |
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AML1/ETO FUSION GENE
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151385 |
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PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY
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151385 |
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RUNT-RELATED TRANSCRIPTION FACTOR 1
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151385 |
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AML1/FOG2 FUSION GENE
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151385 |
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AML1/MDS1 FUSION GENE
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151385 |
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AML1/MDS1/EAI1 FUSION GENE
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151385 |
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AML1/TEL FUSION GENE
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151385 |
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RUNX1/SH3D19 FUSION GENE
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151385 |
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