1 => The disorder is placed on the map based on its association with a gene, but the underlying defect is not known
2 => The disorder has been placed on the map by linkage; no mutation has been found
3 => The molecular basis for the disorder is known; a mutation has been found in the gene
4 => A contiguous gene deletion or duplication syndrome, multiple genes are deleted or duplicated causing the phenotype
| Gene Symbol | Chromosomal Location | Gene MIM number | Mapping Method | Phenotype | Phenotype MIM number | Phenotype Mapping Key |
| CD36 | 7q21.11 | 173510 | A, REc | [Macrothrombocytopenia] (1) | NA | NA |
| CD36 | 7q21.11 | 173510 | A, REc | Platelet glycoprotein IV deficiency, 608404 (3) | 608404 | 3 |
| CD36 | 7q21.11 | 173510 | A, REc | {Malaria, cerebral, susceptibility to}, 611162 (3) | 611162 | 3 |
| CD36 | 7q21.11 | 173510 | A, REc | {Malaria, cerebral, reduced risk of}, 611162 (3) | 611162 | 3 |
| CD36 | 7q21.11 | 173510 | A, REc | {Coronary heart disease, susceptibility to, 7}, 610938 (3) | 610938 | 3 |