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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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acral type peeling skin syndrome
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C536316 |
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sluggishly reacting pupil and hypoactive or absent tendon reflexes tonic
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C531601 |
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CPPDD calcium pyrophosphate dihydrate deposition disease
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C563162 |
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5p13 microduplication syndrome
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13169 |
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autosomal recessive spastic paraplegia 45
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13165 |
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autosomal recessive spastic paraplegia type 45
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13165 |
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autosomal recessive spastic paraplegia type 65
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13165 |
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X-linked, 4 spinocerebellar ataxia
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C537316 |
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x-linked 4 spinocerebellar ataxia
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C537316 |
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progressive, with stapes fixation deafness
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C563316 |
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nonreassuring fetal status
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D005316 |
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X-linked Ataxia-dementia syndrome
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C537316 |
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Cm1 with syringomyelia
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7316 |
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long QT syndrome 1
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100316 |
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long QT syndrome 1, acquired, susceptibility to
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100316 |
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