| 1485 |
Dwarfism, PRKG2-related |
2 |
Animal disease only
|
|
| 1486 |
Night blindness, congenital stationary, LRIT3-related |
1 |
Human gene
|
34.0 |
| 1487 |
Myopia |
3 |
Human disease
|
37.5 |
| 1488 |
Encephalomyelopathy, multifocal symmetrical necrotising, Angus |
1 |
Animal disease only
|
|
| 1489 |
Encephalomyelopathy, multifocal symmetrical necrotising, Limousin |
1 |
Animal disease only
|
|
| 1490 |
Encephalomyelopathy, multifocal symmetrical necrotising, Simmental |
1 |
Animal disease only
|
|
| 1491 |
Tomaculous neuropathy |
1 |
Human disease
|
9.0 |
| 1492 |
Axonopathy, segmental, ALS2-related |
1 |
Target evidence
|
55.5 |
| 1493 |
Porphyria, acute intermittent |
1 |
Target evidence
|
79.1 |
| 1499 |
Aggression |
2 |
Animal disease only
|
|
| 1500 |
Anal sac gland carcinoma |
1 |
Animal disease only
|
|
| 1501 |
Dilute coat color with neurological defects |
2 |
Target evidence
|
57.7 |
| 1502 |
Caprine-like generalized hypoplasia syndrome |
1 |
Human gene
|
29.0 |
| 1503 |
Lysosomal storage disease, ARSG related |
1 |
Animal disease only
|
|
| 1504 |
Neuronal ceroid lipofuscinosis, 1 |
2 |
Target evidence
|
63.4 |
| 1505 |
Neuronal ceroid lipofuscinosis, 10 |
2 |
Target evidence
|
65.1 |
| 1506 |
Neuronal ceroid lipofuscinosis, 8 |
1 |
Target evidence
|
63.2 |
| 1507 |
Incomplete ossification of the humeral condyle |
1 |
Animal disease only
|
|
| 1508 |
Myotubular myopathy 1 |
2 |
Target evidence
|
79.7 |
| 1509 |
Geleophysic dysplasia, ADMATSL2-related |
1 |
Human gene
|
29.0 |
| 1510 |
Tail, wry |
1 |
Animal disease only
|
|
| 1511 |
Contractural arachnodactyly (Fawn calf syndrome) |
1 |
Animal disease only
|
|
| 1512 |
Transitional cell carcinoma |
2 |
Drug
|
62.0 |
| 1513 |
Leukaemia, chronic myelogenous |
2 |
Drug
|
85.8 |
| 1514 |
Acral mutilation syndrome |
1 |
Human disease
|
29.0 |
| 1515 |
Colorectal hamartomatous polyposis and ganglioneuromatosis |
1 |
Target evidence
|
59.6 |
| 1516 |
Gastrointestinal stromal tumour |
1 |
Drug
|
85.2 |
| 1517 |
Retinal atrophy, progressive, X-linked, type 3 |
1 |
Animal disease only
|
|
| 1518 |
Retinal atrophy, progressive, X-linked, type 2 |
1 |
Target evidence
|
53.9 |
| 1519 |
Persistent hyaloid remnants |
1 |
Animal disease only
|
|
| 1520 |
Retinal atrophy - Cone-rod dystrophy 3 |
1 |
Human gene
|
29.0 |
| 1521 |
Retinal atrophy, progressive, CCDC66-related |
1 |
Animal disease only
|
|
| 1522 |
Oculoskeletal dysplasia 1 |
1 |
Human disease
|
9.0 |
| 1523 |
Oculoskeletal dysplasia 2 |
1 |
Human gene
|
29.0 |
| 1524 |
Gallbladder mucoceles |
1 |
Target evidence
|
54.6 |
| 1525 |
Leukocyte adhesion deficiency, type III |
1 |
Target evidence
|
61.7 |
| 1526 |
Factors IX and XII, combined deficiency of |
1 |
Animal disease only
|
|
| 1530 |
Compulsive disorder |
1 |
Human disease
|
34.0 |
| 1534 |
Myxovirus, susceptibility/resistance to |
1 |
Animal disease only
|
|
| 1535 |
Testicular regression syndrome |
1 |
Human disease
|
9.0 |
| 1536 |
Polydactyly, Dorking |
1 |
Animal disease only
|
|
| 1537 |
Polysaccharide storage myopathy, type 2 |
1 |
Animal disease only
|
|
| 1539 |
Pancytopenia, neonatal |
1 |
Animal disease only
|
|
| 1540 |
Ciliary dyskinesia, primary, CCDC39-related |
1 |
Human gene
|
34.0 |
| 1541 |
Arachnomelia, MOCS1-related |
1 |
Target evidence
|
83.1 |
| 1542 |
Hypophosphatemic rickets, autosomal recessive, 1 |
2 |
Human disease
|
14.0 |
| 1543 |
Dyskinesia, paroxysmal |
2 |
Human disease
|
9.5 |
| 1544 |
Hypotrichosis with coat-colour dilution (rat-tail syndrome) |
1 |
Drug
|
49.0 |
| 1546 |
Diplopodia-1 |
1 |
Animal disease only
|
|
| 1547 |
Wingless-2 |
1 |
Drug
|
58.3 |
