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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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DFNB18
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C566580 |
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Del(8)(p23.1)
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16658 |
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arteriolosclerosis
|
6658 |
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papa2
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C566585 |
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8p23.1 deletion
|
16658 |
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deletion 8p23.1
|
16658 |
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monosomy 8p23.1
|
16658 |
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perisylvian syndrome
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C536658 |
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nephronophthisis, infantile
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C566582 |
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chromosome 8p23.1 deletion
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16658 |
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autosomal recessive 18 deafness
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C566580 |
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limb-girdle, type 1e muscular dystrophy
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C566589 |
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postaxial, type a2 polydactyly
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C566585 |
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arteriolosclerosis (morphologic abnormality)
|
6658 |
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familial, 4 arrhythmogenic right ventricular dysplasia
|
C566583 |
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