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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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pfeiffer syndrome 2
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C535578 |
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Heart-hand syndrome 2
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C536784 |
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pseudohypoaldosteronism type 2 caused by mutation in CUL3
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13782 |
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pseudohypoaldosteronism type 2 caused by mutation in Cul3
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13782 |
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pseudohypoaldosteronism type 2 caused by mutation in KLHL3
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13781 |
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pseudohypoaldosteronism type 2 caused by mutation in WNK1
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13778 |
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spastic quadriplegic, 2 cerebral palsy
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C567867 |
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3-Hydroxy-3-Methylglutaryl-CoA synthase 2 deficiency
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C567784 |
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shields type 2 dentin dyspalsia
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D003784 |
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congenital motor, 2 nystagmus
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C537854 |
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paroxysmal familial, 2 ventricular fibrillation
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C567841 |
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hypogonadotropic hypogonadism 2 with or without anosmia
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7844 |
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hypogonadotropic hypogonadism 2 with or without anosmia; HH2
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http://purl.obolibrary.org/obo/MONDO_0007844 |
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CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT
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26782 |
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chondrodysplasia punctata 2, X-linked dominant
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26782 |
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