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MIM:300942 - CHROMOSOME Xq26.3 DUPLICATION SYNDROME
Xenbase Genes: gpr101
Human Disease Resource: MIM
| MONDO:0010491 - X-linked acrogigantism due to Xq26 microduplication |
| MONDO:0017581 - obsolete familial infantile gigantism |
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| MONDO:0010491 - X-linked acrogigantism due to Xq26 microduplication |
| MONDO:0017581 - obsolete familial infantile gigantism |