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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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infantile Canavan disease
|
17830 |
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neonatal Canavan disease
|
17830 |
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severe Canavan disease
|
17830 |
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juvenile Canavan disease
|
17831 |
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mild Canavan disease
|
17831 |
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aortic valve disease 3
|
32783 |
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Mycobacterium xenopi disease or disorder
|
17832 |
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Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
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15783 |
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chromosome 15q11-q13 duplication syndrome
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C557830 |
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Tetra-amelia, ectodermal dysplasia, and lacrimal duct abnormality
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C537838 |
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emery-dreifuss muscular dystrophy 4
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C567831 |
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emery-dreifuss muscular dystrophy 4, autosomal dominant
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C567831 |
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emery-dreifuss muscular dystrophy 5
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C567830 |
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macular corneal dystrophy, type i
|
C537834 |
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TLE6 preimplantation embryonic lethality
|
14783 |
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