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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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Beckwith-Wiedemann syndrome due to 11p15 microdeletion
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0016477 |
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Beckwith-Wiedemann syndrome due to 11p15 microduplication
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0019875 |
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Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion
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0016478 |
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Beckwith-Wiedemann syndrome due to CDKN1C mutation
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0016476 |
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Beckwith-Wiedemann syndrome due to NSD1 mutation
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0016547 |
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Beckwith-Wiedemann syndrome due to imprinting defect of 11p15
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0016475 |
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Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
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0019923 |
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Beemer-Ertbruggen syndrome
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0008857 |
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Beemer-Langer syndrome
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0010024 |
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Behcet disease
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0007191 |
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Behcet syndrome arthropathy
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0002074 |
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Behr syndrome
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0008858 |
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Bell's palsy
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0005665 |
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Bencze syndrome
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0007711 |
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Berardinelli-Seip congenital lipodystrophy
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0018883 |
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