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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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NIPA1 hereditary spastic paraplegia
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10878 |
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congenital laryngeal stridor
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7878 |
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autosomal dominant spastic paraplegia 6
|
10878 |
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keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome
|
18781 |
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3q26 microduplication syndrome
|
19878 |
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Tangier disease; tgd
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http://purl.obolibrary.org/obo/MONDO_0008783 |
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middle lobe syndromes
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D008878 |
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neuroichthyosis hypogonadism syndrome
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C535878 |
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crow fukase syndrome
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D016878 |
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adenosarcoma of the body of uterus
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2878 |
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melanoma of the choroid
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3878 |
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adenosarcoma of the corpus uteri
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2878 |
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Cowden syndrome type 2
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12878 |
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cancer of the skin
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D012878 |
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osteosclerosis of the skull and enlarged mandible
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11878 |
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