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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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CPPDD calcium pyrophosphate dihydrate deposition disease
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C563162 |
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hyperaldosteronism, familial, type i
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C563177 |
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x-linked, with or without seizures, arx-related mental retardation
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C563150 |
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type VII oral-facial-digital syndrome
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C563104 |
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combined, 2 pituitary hormone deficiency
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C563172 |
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spondylometaphyseal dysplasia, richmond type
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C563124 |
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oral-facial-digital syndrome, type VII
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C563104 |
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mental retardation, x-linked 43
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C563150 |
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mental retardation, x-linked 44
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C563137 |
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mental retardation, x-linked 47
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C563151 |
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mental retardation, x-linked 52
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C563150 |
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mental retardation, x-linked 54
|
C563150 |
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mental retardation, x-linked 76
|
C563150 |
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mental retardation, x-linked 87
|
C563150 |
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mental retardation, x-linked 9
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C563137 |
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