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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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structural myopathy, congenital
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D020914 |
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acid lipase deficiency
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19148 |
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ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome
|
9149 |
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chromosome 1q21.1 deletion syndrome
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12914 |
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chromosome 14q32 deletion syndrome
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29143 |
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chromosome 1q21.1 deletion syndrome, 1.35-MB
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12914 |
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hereditary multi-infarct dementia
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914 |
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ectodermal dysplasia-sensorineural deafness syndrome
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9146 |
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Protein C deficiency
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19145 |
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Picornaviridae infectious disease
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5914 |
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Protein C deficiency disease
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19145 |
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CPT 2 deficiency, hepatic
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10914 |
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Anisospondylic camptomicromelic dwarfism Silverman-Handmaker type
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9140 |
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DNA repairs, deficient
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D049914 |
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dystonia musculorum deformans 2
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9141 |
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