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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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3-methylglutaconic aciduria-cataract-neurologic involvement-neutropenia syndrome
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14561 |
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amelogenesis imperfecta, hypoplastic type 1F
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14560 |
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amelogenesis imperfecta hypoplastic type IF
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14560 |
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postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome
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14567 |
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AMBN amelogenesis imperfecta
|
14560 |
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benign sternal neoplasm
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21456 |
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sternum benign neoplasm
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21456 |
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3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia
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14561 |
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benign neoplasm of sternum
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21456 |
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benign tumor of sternum
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21456 |
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glutamate pyruvate transaminase 2 deficiency
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14567 |
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amelogenesis imperfecta type 1F
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14560 |
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amelogenesis imperfecta, type 1F
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14560 |
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Charcot-Marie-Tooth disease type 2 caused by mutation in MARS
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14566 |
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Charcot-Marie-Tooth neuropathy type 2U
|
14566 |
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