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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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Bardet-Biedl syndrome caused by mutation in IFT27
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14447 |
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diarrheal disease, chronic
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44751 |
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testicular germ cell tumor non-seminomatous
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6447 |
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non-dysgerminomatous germ cell tumor of testis
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6447 |
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non-seminomatous germ cell tumor of testis
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6447 |
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pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma
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4478 |
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infection, b. coli
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D001447 |
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autosomal recessive complex SPG due to Kennedy pathway dysfunction
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44737 |
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autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction
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44737 |
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DNAL4 familial congenital mirror movements
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14478 |
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ACER3-related early childhood-onset progressive leukodystrophy
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44718 |
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perihilar intrahepatic cholangiocarcinoma
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44788 |
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Mixed hepatocellular cholangiocarcinoma
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44791 |
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isolated, with coloboma 3 microphthalmia
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C566447 |
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congenital ectodermal defects
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D004476 |
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