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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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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 |
| 489000 |
Ubiquitin-Activating Enzyme, Y-Linked |
| 254090 |
Ullrich Congenital Muscular Dystrophy; UCMD |
| 276820 |
Ulna and Fibula, Absence of, with Severe Limb Deficiency |
| 191400 |
Ulna and Fibula, Hypoplasia of |
| 191420 |
Ulna Metaphyseal Dysplasia Syndrome |
| 276822 |
Ulnar Agenesis and Endocardial Fibroelastosis |
| 608571 |
Ulnar/Fibular Ray Defect and Brachydactyly |
| 191440 |
Ulnar Hypoplasia |
| 314360 |
Ulnar Hypoplasia with Lobster-Claw Deformity of Feet |
| 276821 |
Ulnar Hypoplasia with Mental Retardation |
| 181450 |
Ulnar-Mammary Syndrome; UMS (1 mouse model) |
| 604380 |
Ulnar Ray Dysgenesis with Postaxial Polydactyly and Renal Cystic Dysplasia |
| 609164 |
Umbilicus, Familial Flat |
| 604011 |
Unc119, C. Elegans, Homolog Of; UNC119 |
| 191482 |
Uncombable Hair, Retinal Pigmentary Dystrophy, Dental Anomalies, and Brachydactyly |
| 191480 |
Uncombable Hair Syndrome |
| 191500 |
Undritz Anomaly |
| 608149 |
Uniparental Disomy, Paternal, Chromosome 14 |
| 314380 |
Unique Green Phenomenon |
| 191520 |
Upington Disease |
| 191530 |
Urate-Binding Globulin, Decrease in |
| 191550 |
Ureter, Bifid or Double |
| 191600 |
Ureter, Cancer of |
| 191650 |
Ureterocele |
| 266120 |
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to |
| 191800 |
Urinary Bladder, Atony of |
| 603806 |
Urinary Tract Infections, Recurrent, Susceptibility to |
| 276880 |
Urocanase Deficiency |
| 236730 |
Urofacial Syndrome 1; UFS1 |
| 615112 |
Urofacial Syndrome 2; UFS2 |
| 191700 |
Urolithiasis, Uric Acid, Autosomal Dominant |
| 191850 |
Urticaria, Aquagenic |
| 191950 |
Urticaria, Familial Localized Heat |
| 300280 |
Uruguay Faciocardiomusculoskeletal Syndrome |
| 276904 |
Usher Syndrome, Type Ic; USH1C (4 mouse models) |
| 601067 |
Usher Syndrome, Type ID; USH1D (11 mouse models) |
| 602097 |
Usher Syndrome, Type IE; USH1E |
| 602083 |
Usher Syndrome, Type IF; USH1F (2 mouse models) |
| 606943 |
Usher Syndrome, Type IG; USH1G (3 mouse models) |
| 612632 |
Usher Syndrome, Type IH; USH1H |
| 276901 |
Usher Syndrome, Type IIA; USH2A (1 mouse model) |
| 605472 |
Usher Syndrome, Type IIC; USH2C (3 mouse models) |
| 611383 |
Usher Syndrome, Type Iid; USH2D (1 mouse model) |
| 276902 |
Usher Syndrome, Type IIIA; USH3A (2 mouse models) |
| 614504 |
Usher Syndrome, Type Iiib; USH3B |
| 614869 |
Usher Syndrome, Type IJ; USH1J |
| 614990 |
Usher Syndrome, Type IK; USH1K |
| 276900 |
Usher Syndrome, Type I; USH1 (11 mouse models) |
| 192000 |
Uterine Anomalies |
| 192050 |
Uterus Bicornis Bicollis with Partial Vaginal Septum and Unilateral Hematocolpos with Ipsilateral Renal Agenesis |
| 600630 |
Uv-Sensitive Syndrome 1; UVSS1 |
| 614621 |
Uv-Sensitive Syndrome 2; UVSS2 |
| 614640 |
Uv-Sensitive Syndrome 3; UVSS3 |
| 192100 |
Uvula, Bifid |
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