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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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pediatric embryonal carcinoma of the testis
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3788 |
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Usher syndrome caused by mutation in HARS
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13788 |
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LCD1 lattice corneal dystrophy 1
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C537881 |
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sterol c5-desaturase deficiency
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C537880 |
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pulp disease, dental
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D003788 |
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pulp diseases, dental
|
D003788 |
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dental pulp diseases
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D003788 |
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lattice corneal dystrophy type i
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C537881 |
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CDL1 corneal dystrophy, lattice type 1
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C537881 |
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lattice corneal dystrophy, type i
|
C537881 |
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childhood testicular embryonal carcinoma
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3788 |
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pediatric testicular embryonal carcinoma
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3788 |
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lattice type i corneal dystrophy
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C537881 |
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type i lattice corneal dystrophy
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C537881 |
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corneal dystrophy, lattice type i
|
C537881 |
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