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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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Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology
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0011513 |
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Alzheimer disease, susceptibility to, mitochondrial
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0010783 |
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Ambras type hypertrichosis universalis congenita
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0007787 |
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Amish lethal microcephaly
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0011790 |
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Amobarbital, deficient N-hydroxylation of
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0008775 |
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Anaplasmataceae infectious disease
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0006922 |
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Andersen-Tawil syndrome
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0008222 |
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Angelman syndrome
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0007113 |
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Angelman syndrome due to a point mutation
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0018461 |
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Angelman syndrome due to imprinting defect in 15q11-q13
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0018462 |
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Angelman syndrome due to maternal 15q11q13 deletion
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0020302 |
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Angelman syndrome due to paternal uniparental disomy of chromosome 15
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0020303 |
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Angelucci syndrome
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0001224 |
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Angora hair nevus
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0018258 |
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Anti-neutrophil cytoplasmic antibody-associated vasculitis
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0015492 |
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