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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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autosomal recessive bestrophinopathy
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12733 |
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intellectual disability, autosomal recessive type 40
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14273 |
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mental retardation, autosomal recessive type 40
|
14273 |
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germ cell cancer of the corpus uteri
|
16273 |
|
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papillary thyroid cancers
|
D000077273 |
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nonmedullary thyroid carcinoma
|
D000077273 |
|
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paraganglioma caused by mutation in SDHB
|
7273 |
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colloid extrahepatic bile duct adenocarcinoma
|
2739 |
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colloidal extrahepatic bile duct adenocarcinoma
|
2739 |
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mucinous extrahepatic bile duct adenocarcinoma
|
2739 |
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nonmedullary thyroid carcinomas
|
D000077273 |
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hereditary elliptocytosis caused by mutation in EPB41
|
12731 |
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microcephaly-thin corpus callosum-intellectual disability syndrome
|
14273 |
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complete atrioventricular canal
|
15273 |
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papillary thyroid carcinomas
|
D000077273 |
|
