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| created at |
2021-12-20 02:12:37 UTC |
| updated at |
2021-12-22 07:05:13 UTC |
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MONDO_prefferred_names from the Bioportal site.
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24,286 entries
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There is 0 pattern entry.
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HRPT3
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12406.0 |
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hypertrichotic osteochondrodysplasia Cantu type
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9406.0 |
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adult central nervous system mixed germ cell tumor
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4406.0 |
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chromosome Xp11.22 duplication syndrome
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10406.0 |
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cholesteatoma, congenital
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11406.0 |
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autosomal recessive Emery-Dreifuss muscular dystrophy
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8406.0 |
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obsolete Brown-Vialetto-van Laere syndrome
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406.0 |
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cerebrofacial arteriovenous metameric syndrome type 1
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15406.0 |
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cryofibrinogenemia, familial primary
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7406.0 |
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complete atrioventricular canal-left heart obstruction syndrome
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20406.0 |
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pancreatic agenesis 2
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14406.0 |
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age related macular degeneration 6
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13406.0 |
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rare male infertility due to adrenal disorder of genetic origin
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18406.0 |
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sleep-wake disorder
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3406.0 |
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hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome
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17406.0 |
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