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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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POR deficiency
|
13310 |
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maculopathy, Impg2-related
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13314 |
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Hench's syndrome
|
1332 |
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Hench-Rosenberg syndrome
|
1332 |
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palindromic rheumatism
|
1332 |
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monosomy 16p11.2-p12.2
|
13320 |
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monosomy 16p11.2p12.2
|
13320 |
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FORSYTHE-WAKELING syndrome
|
13321 |
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forsythe-wakeling syndrome
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13321 |
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CDG III
|
13325 |
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COG5-CDG (CDG-III)
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13325 |
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PH III
|
13327 |
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Tsukahara syndrome
|
13332 |
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odontoid hypoplasia
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13333 |
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cocoon syndrome
|
13334 |
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