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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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adenofibroma of body of uterus
|
3458 |
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pharyngeal throat cancer
|
21345 |
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hilar cholangiocellular carcinoma
|
3345 |
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MYOZ2 hypertrophic cardiomyopathy
|
13455 |
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non-familial restrictive cardiomyopathy
|
16345 |
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D-2-hydroxyglutaric aciduria caused by mutation in IDH2
|
13345 |
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retinitis pigmentosa caused by mutation in KIZ
|
14345 |
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hypertrophic cardiomyopathy caused by mutation in MYOZ2
|
13455 |
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osteogenesis imperfecta caused by mutation in SERPINH1
|
13459 |
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Oropouche virus caused disease or disorder
|
345 |
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Schistosoma mansoni caused disease or disorder
|
44345 |
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disease of cochlea
|
3452 |
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disorder of cochlea
|
3452 |
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CRB1 Leber congenital amaurosis
|
13453 |
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IMPDH1 Leber congenital amaurosis
|
13454 |
|
