- OMIM ID
-
141750
- OMIM term:
- ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED
- Alternative terms:
-
ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, DELETION-TYPE
ATR-16 SYNDROME
ATR, DELETION-TYPE
HEMOGLOBIN H-RELATED MENTAL RETARDATION; HBHR
MENTAL RETARDATION WITH HEMOGLOBIN H
CHROMOSOME 16p DELETION SYNDROME
- (∗) Location:
- 16pter-p13.3
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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