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| language |
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| license |
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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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pancreatic agenesis, congenital
|
C564908 |
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pterin-4 alpha-carbinolamine dehydratase 1 deficiency
|
9908 |
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N-acetylglucosaminyltransferase 2 deficiency
|
8908 |
|
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pterin-4 alpha-carbinolamine dehydratase deficiency
|
9908 |
|
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inclusion cell diseases
|
D009081 |
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i cell disease
|
D009081 |
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psuedo hurler disease
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D009081 |
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morquio a disease
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D009085 |
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morquio b disease
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D009085 |
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mossy foot disease
|
15908 |
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post-transplant lymphoproliferative disease
|
19088 |
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glucose metabolism disease
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2908 |
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tuberculosis, extensively drug resistant
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D054908 |
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post-transplant lymphoproliferative disorder
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19088 |
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glucose metabolism disorder
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2908 |
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