| Disease | septooptic dysplasia |
| Comorbidity | C0022735|hypogonadotropic hypogonadism |
| Sentences | 1 |
| PubMedID- 22855648 | Patients with kallmann syndrome (ks; congenital hypogonadotropic hypogonadism and decreased/absent sense of smell), septo-optic dysplasia (sod), or holoprosencephaly (hpe) reportedly have midline defects. |
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