eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | kallmann syndrome |
| Comorbidity | C1535927|charge syndrome |
| Sentences | 1 |
| PubMedID- 21338411 | A unifying hypothesis that could explain both the digeorge syndrome phenotype and the kallman syndrome phenotype in patients with charge syndrome may be that the mutation in chd7 is likely to exert its effect in the common branch of the two pathways of neural crest cells. |
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