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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 articular chondrocalcinosis
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7319 |
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hereditary articular chondrocalcinosis
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7319 |
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sleep initiation dysfunctions
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D007319 |
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dysfunction, sleep initiation
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D007319 |
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calcium gout, familial
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7319 |
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dysfunctions, sleep initiation
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D007319 |
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DIMS (disorders of initiating and maintaining sleep)
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D007319 |
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familial calcium pyrophosphate deposition
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7319 |
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hereditary calcium pyrophosphate deposition
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7319 |
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familial calcium pyrophosphate dihydrate deposition disease
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7319 |
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nystagmus-split hand syndrome
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C537319 |
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torsion, autosomal recessive dystonia 17
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C567319 |
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he
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17319 |
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