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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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autosomal dominant intermediate Charcot-Marie-Tooth disease type D
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11909 |
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pigmentary orthochromatic leukodystrophy
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9096 |
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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
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9096 |
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autosomal dominant leukoencephalopathy with neuroaxonal spheroids
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9096 |
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hereditary diffuse leukoencephalopathy with spheroids
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9096 |
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marden walker like syndrome
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C535909 |
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marden walker like syndrome without psychomotor retardation
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C535909 |
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familial multiple lipomatosis
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7909 |
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adenomyoma of major vestibular gland
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3909 |
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lipomatosis, familial multiple
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7909 |
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autosomal dominant, multiple types 1 cataract
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C566909 |
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syndromic X-linked mental retardation Hough type
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30909 |
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diabetes insipidus nephrogenic mental retardation and intracerebral calcification
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9099 |
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diabetes insipidus, nephrogenic, with intellectual disability and intracerebral calcification
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9099 |
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