(Q3508561)
English
ATR-16 syndrome
alpha thalassemia that has material basis in a deletion in chromosome 16p that involves the alpha-1 (HBA1) and alpha-2 (HBA2) genes, among others
- alpha thalassemia-retardation syndrome
- alpha-thalassemia/mental retardation syndrome, type 1
- ATR syndrome, deletion type
- alpha thalassemia-intellectual disability syndrome, deletion type
- Atr, Deletion-Type
- Hemoglobin H-Related Mental Retardation
- Alpha thalassemia-mental retardation syndrome
- alpha thalassemia-intellectual disability syndrome type 1
- Alpha-thalassemia-intellectual disability syndrome linked to chromosome type 16
- Mental Retardation With Hemoglobin H
- ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED
- ATR syndrome linked to chromosome 16
- alpha-thalassemia-intellectual disability syndrome linked to chromosome 16
- Chromosome 16P Deletion Syndrome
- alpha-thalassemia/mental retardation syndrome, deletion-type
Statements
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282.49
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Identifiers
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Sitelinks
Wikipedia(3 entries)
- dewiki ATR-16-Syndrom
- enwiki ATR-16 syndrome
- frwiki Syndrome ATR 16