Additional Disease Briefs

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corpus callosum agenesis-abnormal genitalia syndrome

Also known as: ACC with abnormal genitalia, ACC-abnormal genitalia syndrome, New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum, Proud Levine Carpenter syndrome, Proud syndrome, Proud-Levine-Carpenter syndrome, corpus callosum, agenesis of, with abnormal genitalia, microcephaly-corpus callosum agenesis-abnormal genitalia syndrome



corpus callosum oligodendroglioma

Also known as: corpus callosum oligodendroglioma, oligodendroglioma of corpus callosumcorpus callosum oligodendroglioma, oligodendroglioma of corpus callosum




corticosteroid-binding globulin deficiency

Also known as: CBG deficiency, Cbg deficiency, Transcortin deficiency, corticosteroid-binding globulin deficiency, corticosteroid-binding globulin, elevated, transcortin deficiency



corticosterone methyloxidase type 1 deficiency

Also known as: 18 Hydroxylase deficiency, 18 alpha hydroxylase deficiency, 18-Hydroxylase deficiency, 18-hydroxycorticosterone dehydrogenase deficiency, 18-hydroxylase deficiency, CAH - 18-hydroxylase deficiency, CMO 1 deficiency, CMO I deficiency, CMO II deficiency, aldosterone deficiency 1, aldosterone deficiency due to 18-hydroxylase defect, aldosterone deficiency due to 18-hydroxysteroid dehydrogenase deficiency, aldosterone deficiency due to defect in 18 hydroxylase, aldosterone deficiency due to defect in steroid 18-Hydroxylase, corticosterone 18-monooxygenase deficiency, corticosterone methyl oxidase type I deficiency, corticosterone methyl oxidase type II deficiency, corticosterone methyloxidase type 1 deficiency, corticosterone methyloxidase type I deficiency, hyperreninemic hypoaldosteronism, familial, 1, hypoaldosteronism, congenital, due to cmo i deficiency, steroid 18-hydroxylase deficiency


corticosterone methyloxidase type 2 deficiency

Also known as: 18-oxidase deficiency, Cmo 2 deficiency, aldosterone deficiency 2, aldosterone deficiency due to deficiency of steroid 18-oxidase, corticosterone methyloxidase type II deficiency, hyperreninemic hypoaldosteronism, familial, 1, hypoaldosteronism, congenital, due to CMO II deficiency, steroid 18-oxidase deficiency