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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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familial Wilms' tumor
|
3321 |
|
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hereditary Wilms tumor
|
3321 |
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hereditary Wilms' tumor
|
3321 |
|
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sialuria, french type
|
C537332 |
|
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polydactyly preaxial type 1
|
C536332 |
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nephrotic syndrome, type 14
|
33203 |
|
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nephrotic syndrome, type 15
|
33262 |
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nephrotic syndrome, type 16
|
33280 |
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Cranioectodermal dysplasia type 2
|
13323 |
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glutaric aciduria type 2, severe neonatal type
|
18332 |
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CDG syndrome type 3
|
13325 |
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hyperoxaluria, primary, type 3
|
13327 |
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primary hyperoxaluria type 3
|
13327 |
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retinitis pigmentosa type 58
|
13328 |
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Senior-Loken syndrome type 7
|
13326 |
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