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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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ARCL3A
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C5234852 |
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P5CS deficiency
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C5234852 |
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Aldehyde dehydrogenase 18 family member A1-related de Barsy syndrome
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C5234852 |
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CUTIS LAXA, CORNEAL CLOUDING, AND MENTAL RETARDATION
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C5234852 |
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CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA
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C5234852 |
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ALDH18A1-related De Barsy syndrome
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C5234852 |
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ALDH18A1-related de Barsy syndrome
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C5234852 |
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Neurocutaneous syndrome Bicknell type
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C5234852 |
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Neurocutaneous syndrome, Bicknell type
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C5234852 |
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neurocutaneous syndrome, Bicknell type
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C5234852 |
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autosomal recessive cutis laxa type IIIA
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C5234852 |
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ALDH18A1-Related Cutis Laxa
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C5234852 |
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PROGEROID SYNDROME OF DE BARSY
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C5234852 |
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cutis laxa, corneal clouding, and intellectual disability
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C5234852 |
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cutis laxa, corneal clouding, and mental retardation
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C5234852 |
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