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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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diabetes insipidus, nephrogenic, with intellectual disability and intracerebral calcification
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9099 |
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diabetes insipidus, nephrogenic, with mental retardation and intracerebral calcification
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9099 |
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partial deletion of the long arm of chromosome 10
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16909 |
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leukoencephalopathy with neuroaxonal spheroids, autosomal dominant
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9096 |
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inborn error of glutathione synthase activity
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17909 |
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congenital disorder of glycosylation type I/IIX
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8909 |
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congenital disorder of glycosylation, type i/IIx
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8909 |
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mother-to-child transmission of Epstein-Barr virus infection
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19094 |
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Dermochondrocorneal dystrophy of François
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9094 |
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subcortical gliosis of Neumann
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9096 |
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partial deletion of chromosome 10q
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16909 |
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partial monosomy of chromosome 10q
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16909 |
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partial monosomy of the long arm of chromosome 10
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16909 |
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partial monosomy of the long arm of chromosome type 10
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16909 |
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polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
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9092 |
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