Additional Disease Briefs

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congenital high-molecular-weight kininogen deficiency

Also known as: Fitzgerald trait, Fitzgerald trait kininogen deficiency, total, included, Flaujeac factor deficiency, Flaujeac trait, Flaujeac trait, included, HMWK, HMWK deficiency, Williams trait, Williams trait, included, high molecular weight kininogen deficiency, high-molecular-weight kininogen deficiency, congenital, kininogen deficiency, kininogen deficiency, high molecular weight, kininogen deficiency, high molecular weight and LOW molecular weight, included, kininogen deficiency, high molecular weight and Low molecular weight, kininogen deficiency, total


congenital Horner syndrome

Also known as: HORNER syndrome, congenital, congenital Claude-Bernard-Horner syndrome, congenital Horner syndrome, congenital Horner syndrome (disease)




congenital hypothyroidism

Also known as: congenital goiter, congenital goitre, congenital hypothyroidism, congenital hypothyroidism not due to iodine deficiency, congenital iodine deficiency syndrome, cretinism, fetal iodine deficiency syndrome, foetal iodine deficiency syndrome, infantile hypothyroidism




congenital hypotrichosis with juvenile macular dystrophy

Also known as: HJMD, Hjmd, hypotrichosis with cone-rod dystrophy, hypotrichosis with juvenile macular degeneration, hypotrichosis with juvenile macular dystrophy, hypotrichosis, congenital, with juvenile macular dystrophy, juvenile macular degeneration and hypotrichosis, juvenile macular dystrophy and congenital hypotrichosis