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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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central polydactyly of hand
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17456 |
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malignant melanoma of the retina
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4561 |
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benign neoplasm of the sternum
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21456 |
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benign tumor of the sternum
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21456 |
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type 2 simpson-golabi-behmel syndrome
|
C564567 |
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melanoma of retina
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4561 |
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paving stone retinal degeneration
|
1456 |
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hereditary, 13 prostate cancer
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C567456 |
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autosomal dominant pure spastic paraplegia caused by mutation in CPT1C
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14568 |
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congenital, with precocious puberty adrenal hypoplasia
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C564568 |
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aphakia, congenital primary
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12456 |
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SCN5A sick sinus syndrome
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24562 |
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autosomal dominant spastic paraplegia 73
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14568 |
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diarrhea, glucose-stimulated secretory, with common variable immunodeficiency
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7456 |
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autosomal dominant spastic paraplegia type 73
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14568 |
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