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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease septooptic dysplasia
Comorbidity C0020619|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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