Human Disease Vocabulary Browser

The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).

Browse vocabulary terms by beginning character

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Human Diseases/Syndromes Beginning with "U"

To see all annotations for a disease, click the disease name.

OMIM ID	Human Disease
OMIM:489000	Ubiquitin-Activating Enzyme, Y-Linked
OMIM:254090	Ullrich Congenital Muscular Dystrophy 1A; UCMD1A
OMIM:620727	Ullrich Congenital Muscular Dystrophy 1B; UCMD1B
OMIM:620728	Ullrich Congenital Muscular Dystrophy 1C; UCMD1C
OMIM:616470	Ullrich Congenital Muscular Dystrophy 2; UCMD2
OMIM:276820	Ulna and Fibula, Absence of, with Severe Limb Deficiency
OMIM:191400	Ulna and Fibula, Hypoplasia of
OMIM:191420	Ulna Metaphyseal Dysplasia Syndrome
OMIM:276822	Ulnar Agenesis and Endocardial Fibroelastosis
OMIM:608571	Ulnar/Fibular Ray Defect and Brachydactyly
OMIM:191440	Ulnar Hypoplasia
OMIM:276821	Ulnar Hypoplasia with Impaired Intellectual Development
OMIM:314360	Ulnar Hypoplasia with Lobster-Claw Deformity of Feet
OMIM:181450	Ulnar-Mammary Syndrome; UMS
OMIM:604380	Ulnar Ray Dysgenesis with Postaxial Polydactyly and Renal Cystic Dysplasia
OMIM:609164	Umbilicus, Familial Flat
OMIM:191482	Uncombable Hair, Retinal Pigmentary Dystrophy, Dental Anomalies, and Brachydactyly
OMIM:191480	Uncombable Hair Syndrome 1; UHS1
OMIM:617251	Uncombable Hair Syndrome 2; UHS2
OMIM:617252	Uncombable Hair Syndrome 3; UHS3
OMIM:191500	Undritz Anomaly
OMIM:314380	Unique Green Phenomenon
OMIM:191520	Upington Disease
OMIM:191530	Urate-Binding Globulin, Decrease in
OMIM:191550	Ureter, Bifid or Double
OMIM:191600	Ureter, Cancer of
OMIM:191650	Ureterocele
OMIM:618477	Uridine-Cytidineuria; URCTU
OMIM:603806	Urinary Tract Infections, Recurrent, Susceptibility to
OMIM:276880	Urocanase Deficiency; UROCD
OMIM:236730	Urofacial Syndrome 1; UFS1
OMIM:615112	Urofacial Syndrome 2; UFS2
OMIM:191700	Urolithiasis, Uric Acid, Autosomal Dominant
OMIM:191850	Urticaria, Aquagenic
OMIM:191950	Urticaria, Familial Localized Heat
OMIM:300280	Uruguay Faciocardiomusculoskeletal Syndrome; FCMSU
OMIM:618632	Usher Syndrome, Type 1M; USH1M
OMIM:276904	Usher Syndrome, Type Ic; USH1C
OMIM:601067	Usher Syndrome, Type ID; USH1D
OMIM:602097	Usher Syndrome, Type IE; USH1E
OMIM:602083	Usher Syndrome, Type IF; USH1F
OMIM:606943	Usher Syndrome, Type IG; USH1G
OMIM:612632	Usher Syndrome, Type IH; USH1H
OMIM:276901	Usher Syndrome, Type IIA; USH2A
OMIM:605472	Usher Syndrome, Type IIC; USH2C
OMIM:611383	Usher Syndrome, Type Iid; USH2D
OMIM:276902	Usher Syndrome, Type IIIA; USH3A
OMIM:614504	Usher Syndrome, Type IIIB; USH3B
OMIM:614869	Usher Syndrome, Type IJ; USH1J
OMIM:614990	Usher Syndrome, Type IK; USH1K
OMIM:276900	Usher Syndrome, Type I; USH1
OMIM:618144	Usher Syndrome, Type IV; USH4
OMIM:619467	Usmani-Riazuddin Syndrome, Autosomal Dominant; USRISD
OMIM:619548	Usmani-Riazuddin Syndrome, Autosomal Recessive; USRISR
OMIM:192000	Uterine Anomalies
OMIM:192050	Uterus Bicornis Bicollis with Partial Vaginal Septum and Unilateral Hematocolpos with Ipsilateral Renal Agenesis
OMIM:600630	Uv-Sensitive Syndrome 1; UVSS1
OMIM:614621	Uv-Sensitive Syndrome 2; UVSS2
OMIM:614640	Uv-Sensitive Syndrome 3; UVSS3
OMIM:192100	Uvula, Bifid

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