| 1792 |
Selective ADP deficiency |
1 |
Animal disease only
|
|
| 1793 |
Feline infectious peritonitis, susceptibility/resistance to |
1 |
Animal disease only
|
|
| 1794 |
Cystic fibrosis |
4 |
Human disease
|
35.0 |
| 1795 |
Niemann-Pick disease, type A |
4 |
Target evidence
|
70.0 |
| 1796 |
Myopathy, congenital, with fibre-type disproportion |
1 |
Human disease
|
9.0 |
| 1797 |
Mast cell tumour |
3 |
Human disease
|
12.5 |
| 1803 |
Endocardial fibroelastosis |
5 |
Human disease
|
15.0 |
| 1804 |
Ocular melanosis |
1 |
Human disease
|
9.0 |
| 1805 |
Amelogenesis imperfecta, ENAM-related |
1 |
Human gene
|
34.0 |
| 1807 |
Leishmaniasis, susceptibility/resistance to |
1 |
Human disease
|
9.0 |
| 1808 |
Multiple autoimmune diseases syndrome |
1 |
Human disease
|
9.0 |
| 1813 |
Haemangiosarcoma |
11 |
Human disease
|
15.0 |
| 1814 |
Congenital chondrodystrophy of unknown origin |
1 |
Animal disease only
|
|
| 1815 |
Autism spectrum disorder |
2 |
Human disease
|
37.0 |
| 1816 |
Superficial digital flexor tendon injury |
1 |
Animal disease only
|
|
| 1817 |
Perinatal weak calf syndrome |
1 |
Human gene
|
29.0 |
| 1818 |
Factor XIII deficiency, F13A1-related |
2 |
Drug
|
65.4 |
| 1819 |
Xanthinuria, type II |
2 |
Target evidence
|
64.4 |
| 1820 |
Ataxia, spinocerebellar, CAPN1-related |
1 |
Human gene
|
34.0 |
| 1821 |
Coat colour, albinism, oculocutaneous type IV |
6 |
Target evidence
|
69.6 |
| 1822 |
Postpartum dysgalactia syndrome |
1 |
Animal disease only
|
|
| 1823 |
Haplotype with homozygous deficiency HH2, IFT80-related |
1 |
Human gene
|
29.0 |
| 1824 |
Haplotype with homozygous deficiency HH3, SMC2-related |
1 |
Animal disease only
|
|
| 1825 |
Haplotype with homozygous deficiency BH1 |
1 |
Animal disease only
|
|
| 1826 |
Haplotype with homozygous deficiency HH4 |
1 |
Animal disease only
|
|
| 1827 |
Haplotype with homozygous deficiency MH1 |
1 |
Animal disease only
|
|
| 1828 |
Haplotype with homozygous deficiency MH2 |
1 |
Animal disease only
|
|
| 1829 |
Haplotype with homozygous deficiency NH5 |
1 |
Animal disease only
|
|
| 1830 |
Haplotype with homozygous deficiency HH7, CENPU-related |
1 |
Animal disease only
|
|
| 1831 |
Haplotype with homozygous deficiency HH8 |
1 |
Animal disease only
|
|
| 1832 |
Haplotype with homozygous deficiency HH9 |
1 |
Animal disease only
|
|
| 1833 |
Haplotype with homozygous deficiency HH11 |
1 |
Animal disease only
|
|
| 1834 |
Haplotype with homozygous deficiency HH10 |
1 |
Animal disease only
|
|
| 1835 |
Haplotype with homozygous deficiency HH12 |
1 |
Animal disease only
|
|
| 1836 |
Haplotype with homozygous deficiency HH13, KIR2DS1-related |
1 |
Animal disease only
|
|
| 1837 |
Haplotype with homozygous deficiency HH14 |
1 |
Animal disease only
|
|
| 1838 |
Haplotype with homozygous deficiency HH15 |
1 |
Animal disease only
|
|
| 1839 |
Haplotype with homozygous deficiency HH16 |
1 |
Animal disease only
|
|
| 1840 |
Haplotype with homozygous deficiency HH17 |
1 |
Animal disease only
|
|
| 1841 |
Distichiasis |
3 |
Animal disease only
|
|
| 1842 |
Haplotype with homozygous deficiency MH3 |
1 |
Animal disease only
|
|
| 1843 |
Haplotype with homozygous deficiency MH4 |
1 |
Animal disease only
|
|
| 1844 |
Haplotype with homozygous deficiency MH5 |
1 |
Animal disease only
|
|
| 1845 |
Haplotype with homozygous deficiency MH6 |
1 |
Animal disease only
|
|
| 1846 |
Haplotype with homozygous deficiency MH7 |
1 |
Animal disease only
|
|
| 1847 |
Haplotype with homozygous deficiency MH8 |
1 |
Animal disease only
|
|
| 1848 |
Haplotype with homozygous deficiency MH9 |
1 |
Animal disease only
|
|
| 1849 |
Haplotype with homozygous deficiency MH10 |
1 |
Animal disease only
|
|
| 1850 |
Haplotype with homozygous deficiency MH11 |
1 |
Animal disease only
|
|
| 1851 |
Haplotype with homozygous deficiency NH1 |
1 |
Animal disease only
|
|
