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| language |
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| license |
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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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haemonchiasis
|
5778 |
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syndromic hypothyroidism
|
15778 |
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gelsolin-related amyloidosis
|
C000657784 |
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kymenlaakso syndrome
|
C000657784 |
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leber congenital amaurosis 4
|
C565778 |
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lattice type II corneal dystrophy
|
C000657784 |
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aipl1-related cone-rod dystrophy
|
C565778 |
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cone-rod dystrophy, aipl1-related
|
C565778 |
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lattice corneal dystrophy type ii
|
C000657784 |
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lattice corneal dystrophy, gelsolin type
|
C000657784 |
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lattice corneal dystrophy, type II
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C000657784 |
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finnish type familial amyloidosis
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C000657784 |
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syndrome associated with hypothyroidism
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15778 |
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familial amyloidosis, finnish type
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C000657784 |
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retinitis pigmentosa, juvenile, aipl1-related
|
C565778 |
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