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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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combined oxidative phosphorylation defect type 29
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33187 |
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autosomal recessive nonsyndromic deafness 106
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33198 |
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autosomal recessive nonsyndromic deafness 107
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33199 |
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moebius congenital oculofacial paralysis
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D020331 |
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malignant tumour of scrotum
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3319 |
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congenital dislocation of, with hyperextensibility of fingers and facial dysmorphism hip
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C563315 |
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sertoli cell only syndrome
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D054331 |
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colorectal (colon or rectal) cancer
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24331 |
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combined deficiency of factor V and factor VIII caused by mutation in MCFD2
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13331 |
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congenital oculofacial paralysis, moebius
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D020331 |
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obsolete skin/hair/eye pigmentation, variation in
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33196.0 |
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carcinoma of parotid
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21331 |
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carcinoma of parotid gland
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21331 |
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torsade DE pointes, short-coupled variant
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13317 |
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ARL6 retinitis pigmentosa
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13312 |
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