Health Conditions
Explore the signs and symptoms, genetic cause, and inheritance pattern of various health conditions.
- ubiquinone deficiency, see primary coenzyme Q10 deficiency
- ubiquinone-cytochrome c oxidoreductase deficiency, see mitochondrial complex III deficiency
- UC, see ulcerative colitis
- UDA syndrome, see Muckle-Wells syndrome
- Udd distal myopathy, see tibial muscular dystrophy
- Udd myopathy, see tibial muscular dystrophy
- Udd-Markesbery muscular dystrophy, see tibial muscular dystrophy
- UDP-galactose-4-epimerase deficiency disease, see galactosemia
- UFS, see Ochoa syndrome
- UHS, see uncombable hair syndrome
- ulcerative colitis
- ULD, see Unverricht-Lundborg disease
- Ullrich-Feichtiger syndrome, see Fraser syndrome
- Ullrich-Noonan syndrome, see Noonan syndrome
- Ullrich-Turner syndrome, see Turner syndrome
- ultraviolet sensitive syndrome, see UV-sensitive syndrome
- UMAK, see uromodulin-associated kidney disease
- UMOD-related kidney disease, see uromodulin-associated kidney disease
- uncombable hair syndrome
- unconjugated benign bilirubinemia, see Gilbert syndrome
- unilateral defect of pectoralis major and syndactyly of the hand, see Poland syndrome
- unilateral intrauterine facial necrosis, see craniofacial microsomia
- unilateral mandibulofacial dysostosis, see craniofacial microsomia
- unmanageable hair syndrome, see uncombable hair syndrome
- Unverricht-Lundborg disease
- Unverricht-Lundborg syndrome, see Unverricht-Lundborg disease
- Urbach-Wiethe disease, see lipoid proteinosis
- Urbach-Wiethe lipoid proteinosis, see lipoid proteinosis
- Urbach-Wiethe syndrome, see lipoid proteinosis
- Urinary bladder cancer, see bladder cancer
- urofacial Ochoa's syndrome, see Ochoa syndrome
- urofacial syndrome, see Ochoa syndrome
- Uromodulin storage disease, see uromodulin-associated kidney disease
- uromodulin-associated kidney disease
- urticaria-deafness-amyloidosis syndrome, see Muckle-Wells syndrome
- Usher syndrome
- Usher's syndrome, see Usher syndrome
- usual interstitial pneumonia, see idiopathic pulmonary fibrosis
- UTP hexose-1-phosphate uridylyltransferase deficiency, see galactosemia
- UV-sensitive syndrome
- uveoretinal coloboma, see coloboma
- UVSS, see UV-sensitive syndrome
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