Additional Disease Briefs

typical urticaria pigmentosa

tyrosinemia type II

Also known as: Oregon type tyrosinemia, Richner Hanhart syndrome, Richner-Hanhart syndrome, TYRSN2, Tat deficiency, Tyrosinosis oculocutaneous type, Tyrosinosis, oculocutaneous type, keratosis palmoplantaris with corneal dystrophy, keratosis palmoplantaris-corneal dystrophy syndrome, oculocutaneous tyrosinemia, tyrosine aminotransferase deficiency, tyrosine transaminase deficiency, tyrosinemia due to TAT deficiency, tyrosinemia due to tyrosine aminotransferase deficiency, tyrosinemia type 2, tyrosinemia type II, tyrosinemia, type 2, tyrosinemia, type II

tyrosinemia type III

Also known as: 4-Hydroxyphenylpyruvate dioxygenase deficiency, 4-Hydroxyphenylpyruvic acid oxidase deficiency, 4-alpha hydroxyphenylpyruvate dioxygenase deficiency, 4-alpha hydroxyphenylpyruvic acid oxidase deficiency, TYRSN3, tyrosinemia due to 4-hydroxyphenylpyruvate dioxygenase deficiency, tyrosinemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency, tyrosinemia due to HPD deficiency, tyrosinemia type 3, tyrosinemia type III, tyrosinemia, type 3, tyrosinemia, type III

Uhl anomaly

Also known as: Uhl's anomaly, parchment right ventricle

Ulbright-Hodes syndrome

Also known as: RL syndrome, Ulbright Hodes syndrome, renal dysplasia limb defects syndrome, renal dysplasia, mesomelia, and radiohumeral fusion, renal dysplasia-limb defects syndrome, renal dysplasia-mesomelia-radiohumeral fusion syndrome

ulerythema ophryogenesis

Also known as: keratosis pilaris affecting the follicles of the eyebrow hairs, type of genodermatosis

Ullrich congenital muscular dystrophy

Also known as: UCMD, Ullrich disease, Ullrich scleroatonic muscular dystrophy, congenital muscular dystrophy, Ullrich type, late onset scleroatonic familial myopathy (subtype), scleroatonic Ullrich disease, scleroatonic muscular dystrophyUCMD, Ullrich disease, Ullrich scleroatonic muscular dystrophy, congenital muscular dystrophy, Ullrich type, late onset scleroatonic familial myopathy (subtype), scleroatonic Ullrich disease, scleroatonic muscular dystrophy

ulna metaphyseal dysplasia syndrome

Also known as: Rosenberg Lohr syndrome, Rosenberg-Lohr syndrome, hereditary bone dysplasia with characteristic bowing and thickening of the distal ulna, metaphyseal chondrodysplasia, Rosenberg type, metaphyseal chondroplasia Rosenberg type, ulna metaphyseal dysplasia syndrome

ulnar hemimelia

Also known as: congenital longitudinal deficiency of the ulna, ulnar clubhand, ulnar longitudinal meromelia