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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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nystagmus with congenital zonular cataract
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C536727 |
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t-cell immunodeficiency, congenital alopecia, and nail dystrophy
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C536781 |
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pharyngeal adenoid cystic carcinoma
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6367 |
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pharynx adenoid cystic carcinoma
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6367 |
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x-linked, with congenital contractures and low fingertip arches mental retardation
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C536703 |
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oculomotor, with congenital contractures and muscle atrophy apraxia
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C536703 |
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Zeta-associated-protein 70 deficiency
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C536722 |
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selective t-cell defect
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C536722 |
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carnitine uptake deficiency
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C536778 |
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sagittal, with dandy-walker malformation and hydrocephalus craniosynostosis
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C536790 |
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sagittal craniosynostosis, dandy-walker malformation, and hydrocephalus
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C536790 |
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systemic carnitine deficiency
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C536778 |
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TMEM43 autosomal dominant Emery-Dreifuss muscular dystrophy
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13677 |
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yemenite (warburg) deaf-blind hypopigmentation syndrome
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C536771 |
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chromosome 15q25 deletion syndrome
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13672 |
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