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| license |
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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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JET
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17989 |
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Mcor
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7989 |
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congenital microcoria
|
7989 |
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congenital miosis
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7989 |
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microcoria, congenital
|
7989 |
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miosis, congenital
|
7989 |
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pinhole pupils
|
7989 |
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CMT 2b
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C537989 |
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autosomal dominant (PSN) peripheral sensory neuropathy
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C537989 |
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axonal, type 2b charcot-marie-tooth disease
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C537989 |
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neuronal, type 2b charcot-marie-tooth disease
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C537989 |
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hereditary motor and sensory neuropathy IIB
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C537989 |
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hereditary motor and sensory neuropathy 2 b (HMSN 2 b)
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C537989 |
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charcot-marie-tooth disease, autosomal dominant, type 2b
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C537989 |
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charcot-marie-tooth disease, axonal, type 2b
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C537989 |
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