About   Help   FAQ
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
 
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
 

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, C. Elegans, Homolog Of; 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: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
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: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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
09/12/2017
MGI 6.10
The Jackson Laboratory