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Disease	Synonyms	Description	Articles	Phenotypes
schwannoma of ureter	ureteral schwannoma	n_a
Vogt-Koyanagi-Harada disease	uveomeningoencephalitic syndrome; Harada's disease.. [+] uveomeningoencephalitic syndrome; Harada's disease; Vogt-Koyanagi syndrome; Vogt-Koyanagi-Harada disease (disorder) [-]	A hypersensitivity reaction type II disease that i..[+] A hypersensitivity reaction type II disease that is caused by T helper cell mediated autoimmune attack of melanocytes resulting in inflammation of the inside of the eye, whitening of hair, skin pigment loss, and meningitis. [-]
prolapse of urethra	Urethrocele	n_a
posterior uveitis	Uveitis, posterior	n_a
deficiency anemia	Unspecified deficiency anemia; deficiency anemias .. [+] Unspecified deficiency anemia; deficiency anemias (disorder); deficiency anemias NOS (disorder) [-]	n_a
acute cystitis	urinary tract infection	A cystitis characterized by a sudden onset or seve..[+] A cystitis characterized by a sudden onset or severe symptoms. [-]
chancroid	Ulcus molle, skin; (Chancroid [& bubo]) or (Ducrey.. [+] Ulcus molle, skin; (Chancroid [& bubo]) or (Ducrey's chancre) [-]	A primary bacterial infectious disease that is a s..[+] A primary bacterial infectious disease that is a sexually transmitted infection located in skin of the genitals, has_material_basis_in Haemophilus ducreyi, which is transmitted by sexual contact. The infection has symptom painful and soft ulcers. [-]
interstitial cystitis	ulcerative cystitis	n_a
lipoid proteinosis	URBACH-WIETHE DISEASE; Lipid proteinosis (disorder.. [+] URBACH-WIETHE DISEASE; Lipid proteinosis (disorder); Lipoid proteinosis [-]	n_a
nonepidermolytic palmoplantar keratoderma	Unna-Thost Syndrome; diffuse nonepidermolytic palm.. [+] Unna-Thost Syndrome; diffuse nonepidermolytic palmomplantar keratoderma; Thost-Unna Syndrome; tylosis [-]	A palmoplantar keratosis characterized by a well-d..[+] A palmoplantar keratosis characterized by a well-demarcated, symmetric keratoderma located_in palms and located_in soles. [-]
endemic typhus	urban typhus; Urban Typhus of Malaya; cat flea ric.. [+] Urban Typhus of Malaya; urban typhus; cat flea rickettsiosis; fleaborne typhus; murine typhus; Rat-Flea Typhus; Rickettsia felis spotted fever; Shop typhus; toulon typhus [-]	A typhus that has_material_basis_in Rickettsia typ..[+] A typhus that has_material_basis_in Rickettsia typhi or has_material_basis_in Rickettsia felis, which are transmitted_by fleas (Xenopsylla cheopis). The infection has_symptom headache, has_symptom fever, has_symptom chills, has_symptom myalgia, has_symptom nausea, has_symptom vomiting, has_symptom cough and has_symptom rash. [-]
gastroduodenal Crohn's disease	upper GI Crohn's disease	An inflammatory bowel disease characterized by inf..[+] An inflammatory bowel disease characterized by inflammation located_in stomach and located_in duodenum, has_symptom nausea, has_symptom vomiting, has_symptom weight loss and has_symptom loss of appetite. [-]
overactive bladder syndrome	urge syndrome; urgency-frequency syndrome; OAB; ov.. [+] urgency-frequency syndrome; urge syndrome; OAB; overactive bladder [-]	A bladder disease characterized by urinary urgency..[+] A bladder disease characterized by urinary urgency without urinary tract infection or obvious pathology, usually accompanied by urinary frequency and nocturia. [-]
apparent mineralocorticoid excess	Ulick syndrome; 11-beta-hydroxysteroid dehydrogena.. [+] Ulick syndrome; 11-beta-hydroxysteroid dehydrogenase deficiency type 2; APE; cortisol 11-beta-ketoreductase deficiency [-]	An adrenal gland hyperfunction characterized by de..[+] An adrenal gland hyperfunction characterized by decreased conversion of biologically active cortisol to inactive cortisone resulting in low aldosterone levels, metabolic alkalosis, hypernatremia, hypokalemia and early-onset severe hypertension that has_material_basis_in homozygous or compound heterozygous mutation in the HSD11B2 gene on chromosome 16. [-]
arrhythmogenic right ventricular dysplasia 1	Uhl anomaly; arrhythmogenic right ventricular card.. [+] Uhl anomaly; arrhythmogenic right ventricular cardiomyopathy 1; ARVC1; ARVD1; familial arrhythmogenic right ventricular dysplasia 1 [-]	An arrhythmogenic right ventricular dysplasia that..[+] An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the TGFB3 gene on chromosome 14q24. [-]
autosomal dominant nonsyndromic deafness 69	unilateral or asymmetric congenital deafness; auto.. [+] unilateral or asymmetric congenital deafness; autosomal dominant deafness 69; DCUA; DFNA69 [-]	An autosomal dominant nonsyndromic deafness that h..[+] An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21. [-]
tibial muscular dystrophy	Udd myopathy; Udd type distal myopathy; distal tit.. [+] Udd type distal myopathy; Udd myopathy; distal titinopathy; Finnish tibial muscular dystrophy; Tardive tibial muscular dystrophy; TMD [-]	A distal muscular dystrophy characterized by autos..[+] A distal muscular dystrophy characterized by autosomal dominant inheritance of late-onset muscular dystrophy beginning in the anterior comparment of the legs that has_material_basis_in heterozygous mutation in the TTN gene on chromosome 2q31. [-]
Mulchandani-Bhoj-Conlin syndrome	UPD(20)mat; maternal uniparental disomy of chromos.. [+] UPD(20)mat; maternal uniparental disomy of chromosome 20; maternal UPD(20); MBCS [-]	A syndrome characterized by prenatal growth restri..[+] A syndrome characterized by prenatal growth restriction, severe short stature with proportional head circumference, and profound feeding difficulty that has_material_basis_in heterozygous mutation in an imprinting region on chromosome 20q11-q13. [-]

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