| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 4q13.3 | Chopra-Amiel-Gordon syndrome | 619504 | AD | 3 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 4q13.3 | Chopra-Amiel-Gordon syndrome | 619504 | AD | 3 | ANKRD17 | 615929 |
|
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|
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