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

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Human Diseases/Syndromes Beginning with "U"

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

OMIM IDHuman Disease
OMIM:489000 Ubiquitin-Activating Enzyme, Y-Linked
OMIM:254090 Ullrich Congenital Muscular Dystrophy 1; UCMD1
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:314360 Ulnar Hypoplasia with Lobster-Claw Deformity of Feet
OMIM:276821 Ulnar Hypoplasia with Mental Retardation
OMIM:181450 Ulnar-Mammary Syndrome; UMS
OMIM:604380 Ulnar Ray Dysgenesis with Postaxial Polydactyly and Renal Cystic Dysplasia
OMIM:609164 Umbilicus, Familial Flat
OMIM:604011 Unc119 Lipid-Binding Chaperone; UNC119
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:266120 Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to
OMIM:618477 Uridine-Cytidineuria; URCTU
OMIM:191800 Urinary Bladder, Atony of
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: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

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.14
The Jackson Laboratory