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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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autosomal recessive non-syndromic intellectual disability caused by mutation in CRADD
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13785 |
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congenital disorder of glycosylation type 1r
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13789 |
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congenital disorder of glycosylation type Ir
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13789 |
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congenital disorder of glycosylation, type Ir
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13789 |
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congenital disorder of glycosylation, type Ir; CDG1R
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http://purl.obolibrary.org/obo/MONDO_0013789 |
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malignant neoplasm of urachus
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1378 |
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malignant tumor of urachus
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1378 |
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CRADD autosomal recessive non-syndromic intellectual disability
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13785 |
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lethal neonatal rigidity-multifocal seizure syndrome
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13784 |
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lethal neonatal spasticity-epileptic encephalopathy syndrome
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13784 |
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HARS Usher syndrome
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13788 |
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dejerine roussy syndrome
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D013786 |
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neoplasm of the endocardium
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21378 |
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tumor of the endocardium
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21378 |
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cone-rod dystrophy type 16
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13786 |
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