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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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osteopetrosis (disease), autosomal recessive
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19026 |
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Charcot-Marie-Tooth disease, demyelinating, type 1F; CMT1F
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http://purl.obolibrary.org/obo/MONDO_0011902 |
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pediatric autoimmune disorders associated with Streptococcus infections
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19020 |
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NEFL Charcot-Marie-Tooth disease type 1
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11902 |
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Charcot-Marie-Tooth disease type 1F
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11902 |
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segmental odontomaxillary dysplasia
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19029 |
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SOD
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19029 |
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autosomal recessive malignant osteopetrosis
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19026 |
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sarcoma of mast cell
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19024 |
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cutaneous (skin) mastocytosis
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19023 |
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mast cell sarcoma
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19024 |
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amoebiasis due to Entamoeba histolytica
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19028 |
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sensorineural hearing loss-early graying-essential tremor syndrome
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19022 |
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pediatric autoimmune neuropsychiatric disorder associated with Streptococcus
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19020 |
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pediatric autoimmune neuropsychiatric disorders associated with Streptococcus infections
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19020 |
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