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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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USH3B
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13788 |
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3-beta-hydroxysteroid-delta(5)-desaturase deficiency
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C537880 |
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biber-haab-dimmer dystrophy
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C537881 |
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peters anomaly
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C537884 |
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pfeiffer-palm-teller syndrome
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C537889 |
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deficiency of 3-beta-hydroxysteroid-delta(5)-desaturase
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C537880 |
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rhabdomyosarcoma embryonal 1
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C537883 |
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lattice type 1 CDL1 corneal dystrophy
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C537881 |
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lattice type 1 corneal dystrophy
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C537881 |
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testicular embryonal carcinoma of childhood
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3788 |
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posterior polymorphous, 3 corneal dystrophy
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C563788 |
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mental retardation and multiple dysmorphisms short stature
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C537887 |
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childhood embryonal carcinoma of testis
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3788 |
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pediatric embryonal carcinoma of testis
|
3788 |
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childhood embryonal carcinoma of the testis
|
3788 |
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