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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.
X-linked spinocerebellar ataxia type 4
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0010534 |
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X-linked spondyloepimetaphyseal dysplasia
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0010248 |
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X-linked syndromic intellectual disability
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0020119 |
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XFE progeroid syndrome
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0012590 |
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XH antigen
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0010760 |
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XK aprosencephaly
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0008811 |
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XY type gonadal dysgenesis-associated anomalies syndrome
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0009302 |
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XYLT1-CDG
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0018273 |
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Xp22.13p22.2 duplication syndrome
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0017284 |
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Xp22.3 microdeletion syndrome
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0015606 |
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Xq12-q13.3 duplication syndrome
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0017794 |
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Xq25 microduplication syndrome
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0010507 |
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Xq27.3q28 duplication syndrome
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0010467 |
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Y chromosome infertility due to DAZ1 deletion
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0042605 |
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Y chromosome number anomaly
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0017005 |
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