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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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ARTHS
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C4225396 |
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MRD32
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C4225396 |
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autosomal dominant intellectual disability 32
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C4225396 |
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ARBOLEDA-THAM SYNDROME
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C4225396 |
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Arboleda-Tham syndrome
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C4225396 |
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KAT6A SYNDROME
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C4225396 |
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KAT6A Syndrome
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C4225396 |
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KAT6A syndrome
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C4225396 |
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MRD32, FORMERLY
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C4225396 |
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MENTAL RETARDATION, AUTOSOMAL DOMINANT 32, FORMERLY
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C4225396 |
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Mental retardation, autosomal dominant 32
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C4225396 |
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intellectual disability, autosomal dominant 32
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C4225396 |
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mental retardation, autosomal dominant 32
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C4225396 |
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intellectual disability, autosomal dominant type 32
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C4225396 |
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mental retardation, autosomal dominant type 32
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C4225396 |
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