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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 "X"
To see all annotations for a disease, click the disease name.
| OMIM ID |
Human Disease |
| 278300 |
Xanthinuria, Type I |
| 603592 |
Xanthinuria, Type II |
| 602247 |
Xanthomatosis, Susceptibility to |
| 194400 |
Xeroderma Pigmentosum, Autosomal Dominant, Mild |
| 278700 |
Xeroderma Pigmentosum, Complementation Group A; XPA (1 mouse model) |
| 610651 |
Xeroderma Pigmentosum, Complementation Group B; XPB (1 mouse model) |
| 278720 |
Xeroderma Pigmentosum, Complementation Group C; XPC (1 mouse model) |
| 278730 |
Xeroderma Pigmentosum, Complementation Group D; XPD (1 mouse model) |
| 278740 |
Xeroderma Pigmentosum, Complementation Group E (4 mouse models) |
| 278760 |
Xeroderma Pigmentosum, Complementation Group F; XPF (1 mouse model) |
| 278780 |
Xeroderma Pigmentosum, Complementation Group G; XPG (4 mouse models) |
| 278750 |
Xeroderma Pigmentosum, Variant Type; XPV (3 mouse models) |
| 610965 |
Xfe Progeroid Syndrome (1 mouse model) |
| 314800 |
Xh Antigen |
| 300113 |
X-Linked B Cell Surface Antigen, Mouse, Homolog-Like 1; XLRL |
| 300145 |
X-Prolyl Aminopeptidase 2; XPNPEP2 |
| 278900 |
Xylosidase Deficiency |
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