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| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
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MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
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622,528 entries
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There is 0 pattern entry.
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ASNSD
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C3809971 |
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Asparagine synthetase deficiency
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C3809971 |
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ASNS DEFICIENCY
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C3809971 |
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Asns deficiency
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C3809971 |
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Asparagine Synthetase Deficiency
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C3809971 |
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Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
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C3809971 |
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congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
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C3809971 |
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ASPARAGINE SYNTHETASE DEFICIENCY
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C3809971 |
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asparagine synthetase deficiency
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C3809971 |
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Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome
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C3809971 |
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Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome
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C3809971 |
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