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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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congenital EBV infection
|
19094 |
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hereditary diffuse leukoencephalopathy with axonal spheroids
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9096 |
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hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia
|
9096 |
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autosomal dominant leukoencephalopathy with neuroaxonal spheroids
|
9096 |
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hereditary diffuse leukoencephalopathy with spheroids
|
9096 |
|
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marden walker like syndrome
|
C535909 |
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marden walker like syndrome without psychomotor retardation
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C535909 |
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familial multiple lipomatosis
|
7909 |
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syndromic X-linked mental retardation Hough type
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30909 |
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adenomyoma of major vestibular gland
|
3909 |
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Pestivirus disease or disorder
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5909 |
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mother-to-child transmission of Epstein-Barr virus infection
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19094 |
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Dermochondrocorneal dystrophy of François
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9094 |
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subcortical gliosis of Neumann
|
9096 |
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partial deletion of chromosome 10q
|
16909 |
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