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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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DOCK8 deficiency
|
9478 |
|
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melanosis, neurocutaneous
|
9578 |
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neurocutaneous melanocytosis
|
9578 |
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neurocutaneous melanosis
|
9578 |
|
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snyder-robinson syndrome
|
C536678 |
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muscle-eye-brain-FKTN related
|
9678 |
|
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tabatznik syndrome
|
C536784 |
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Czeizel syndrome
|
9780 |
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onycho-tricho-dysplasia-neutropenia syndrome
|
9781 |
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Costeff syndrome
|
9787 |
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OPA3 defect
|
9787 |
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baller-gerold syndrome
|
C536788 |
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gemignani syndrome
|
C537678 |
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Hanhart dwarfism
|
9878 |
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HMGCS2 deficiency
|
C567784 |
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