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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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APCA
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7163 |
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CAPA
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7163 |
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EA2
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7163 |
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PANDAS pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections
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C537163 |
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episodic ataxia, Nystagmus-associated
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7163 |
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autosomal dominant PROC deficiency
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C567163 |
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PROC deficiency, autosomal dominant
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C567163 |
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autosomal dominant protein c deficiency
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C567163 |
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Nystagmus-associated episodic ataxia
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7163 |
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familial paroxysmal ataxia
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7163 |
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hereditary episodic ataxia caused by mutation in CACNA1A
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7163 |
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Acetazolamide-responsive episodic ataxia syndrome
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7163 |
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protein c deficiency, autosomal dominant
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C567163 |
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hemolytic disease of the fetus and newborn
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17163 |
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Cerebellopathy, hereditary paroxysmal
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7163 |
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