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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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ANIB9
|
12949.0 |
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mitochondrial complex 4 deficiency, nuclear type 14
|
33649.0 |
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optic atrophy 12
|
33549.0 |
|
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pityriasis lichenoides
|
24249.0 |
|
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infection due to clostridium perfringens
|
23149.0 |
|
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cerebral visual impairment
|
18649.0 |
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obsolete rare renal tumor
|
19749.0 |
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polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1
|
20749.0 |
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alopecia macular degeneration growth retardation syndome
|
21849.0 |
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ovarian dysgenesis 2
|
10349.0 |
|
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peroxisome biogenesis disorder 10b
|
54549.0 |
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hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
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18749.0 |
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isolated micropenis
|
19849.0 |
|
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obsolete Charcot-Marie-Tooth disease type 1
|
349.0 |
|
|
intracranial hemorrhage
|
5049.0 |
|
