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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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Groenouw type II corneal dystrophy
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9020 |
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autosomal recessive MSMD due to partial IFNgammaR2 deficiency
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17902 |
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autosomal recessive MSMD due to partial interferon gamma receptor 2 deficiency
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17902 |
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mast cell activation syndromes
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D000090267 |
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spondyloepiphyseal dysplasia, Reardon type
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10902 |
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type 2e Limb-girdle muscular dystrophy
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C535902 |
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liver cell adenoma
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18902 |
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occipitotemporal lobe, and migraine with aura epilepsy
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C566902 |
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cramps, familial adolescent
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9027 |
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corpus callosum agenesis
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9022 |
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corpus callosum agenesis facial anomalies Robin sequence
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9021 |
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corpus callosum agenesis neuronopathy
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902 |
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corpus callosum, agenesis of
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9022 |
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cleft Lip/palate, agenesis of clavicles and cervical vertebrae, and talipes equinovarus
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9028 |
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corpus callosum, agenesis of, with facial anomalies and ROBIN sequence
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9021 |
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