syndromic intellectual disability syndromic disease hematologic disorder alpha thalassemia-intellectual disability syndrome type 1 https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/6746 https://www.malacards.org/card/alpha_thalassemia_impaired_intellectual_development_syndrome_deletion_type https://www.malacards.org/card/alpha_thalassemia_intellectual_disability_syndrome_type_1 GARD:0016862 Haemoglobin H-related mental retardation Alpha-thalassemia-intellectual deficit syndrome linked to chromosome 16 (ATR-16), a contiguous gene deletion syndrome, is a form of alpha-thalassemia characterized by microcytosis, hypochromia, normal hemoglobin (Hb) level or mild anemia, associated with developmental abnormalities. Alpha-thalassemia/mental retardation syndrome, deletion-type DECIPHER:65 Haemoglobin H-related intellectual disability MONDO:0007716 alpha-thalassemia-intellectual disability syndrome linked to chromosome 16 NORD:1879 ALPHA-thalassemia/mental retardation syndrome, chromosome 16-related UMLS:C0795917 intellectual disability with Haemoglobin H Alpha-thalassemia-intellectual disability syndrome linked to chromosome type 16 alpha-thalassemia/intellectual disability syndrome, deletion-type MEDGEN:162892 ICD9:282.49 MESH:C563050 Alpha thalassemia-intellectual disability syndrome, deletion type alpha-thalassemia/intellectual disability syndrome, type 1 ATR syndrome linked to chromosome 16 alpha thalassemia-intellectual disability syndrome, deletion type OMIM:141750 Alpha thalassemia-mental retardation syndrome DOID:0110029 ATR-16 syndrome ATR syndrome, deletion type ATR-16 Syndrome Alpha thalassemia-intellectual disability syndrome alpha-thalassemia/mental retardation syndrome, deletion-type SCTID:277918006 mental retardation with Hemoglobin H mental retardation with Haemoglobin H Hemoglobin H-related mental retardation Orphanet:98791 partial deletion of the short arm of chromosome 16