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| language |
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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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methemoglobinemia, type i
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C537841 |
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methemoglobinemia, type ii
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C537841 |
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nasal cavity in situ carcinoma
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3784 |
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emmonsia crescens infection
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C000656784 |
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familial Joint instability syndrome
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7842 |
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familial joint instability syndrome
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7842 |
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disease of intervertebral joint
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37847 |
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disorder of intervertebral joint
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37847 |
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disorder of joint of spine
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37847 |
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autosomal dominant keratitis
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7848 |
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dominantly inherited keratitis
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7848 |
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gelsolin type lattice corneal dystrophy
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C000657784 |
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type II lattice corneal dystrophy
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C000657784 |
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corneal dystrophy, lattice type II
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C000657784 |
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familial joint laxity
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7842 |
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