| 2365 |
Cardiomyopathy, dilated, RBM20-related |
2 |
Target evidence
|
58.2 |
| 2366 |
Forebrain commissural malformation, ventriculomegaly and interhemispheric cysts, GDF7-related |
1 |
Animal disease only
|
|
| 2367 |
Ataxia, cerebellar, SELENOP-related |
1 |
Animal disease only
|
|
| 2368 |
Ichthyosis, ABHD5-related |
1 |
Target evidence
|
57.8 |
| 2369 |
Hygroma, cystic |
1 |
Human disease
|
9.0 |
| 2370 |
Motor neuron disease, TMCO6-related |
1 |
Animal disease only
|
|
| 2371 |
Microcephaly, MFSD2A-related |
1 |
Target evidence
|
58.4 |
| 2372 |
Haemoglobinuria, paroxysmal nocturnal |
1 |
Human disease
|
5.0 |
| 2374 |
Charcot Marie Tooth disease, FGD4-related |
1 |
Target evidence
|
55.2 |
| 2375 |
Congenital disorder of glycosylation, GALNT2-related |
1 |
Target evidence
|
56.2 |
| 2376 |
Heart defect, congenital, SAP130-related |
1 |
Animal disease only
|
|
| 2378 |
Parkinson disease, SNCA-related |
4 |
Human disease
|
30.0 |
| 2379 |
Parkinson disease, LRRK2-related |
1 |
Human disease
|
5.0 |
| 2380 |
Thyroid follicular cell carcinoma, predisposition to |
1 |
Drug
|
33.1 |
| 2381 |
Skeletal-cardio-enteric dysplasia, MAP2K2-related |
1 |
Human gene
|
29.0 |
| 2382 |
Afibrinogenaemia, FGA-related |
1 |
Human disease
|
26.5 |
| 2383 |
Ornithine transcarbamylase deficiency |
1 |
Human disease
|
30.0 |
| 2384 |
Hypercalciuria, idiopathic |
1 |
Human disease
|
11.5 |
| 2389 |
Spinal muscular atrophy, LIX1-related |
1 |
Animal disease only
|
|
| 2390 |
Spinal muscular atrophy, KDSR-related |
1 |
Animal disease only
|
|
| 2391 |
Pyometra, predisposition to |
1 |
Animal disease only
|
|
| 2392 |
Liver fibrosis, congential, generic |
1 |
Animal disease only
|
|
| 2393 |
Keratoconjunctivitis sicca |
1 |
Human disease
|
31.5 |
| 2394 |
Cleft lip, GADD45G-related |
1 |
Animal disease only
|
|
| 2395 |
Haplotype with homozygous deficiency, AA14H3 |
1 |
Animal disease only
|
|
| 2396 |
Haplotype with homozygous deficiency, CH19H2 |
1 |
Animal disease only
|
|
| 2397 |
Haplotype with homozygous deficiency, SI16H5 |
1 |
Animal disease only
|
|
| 2398 |
Neuropathy and feather colour, dilution |
1 |
Animal disease only
|
|
| 2399 |
Cryptophthalmos |
1 |
Human disease
|
9.0 |
| 2402 |
Phelan-McDermid syndrome |
2 |
Human disease
|
25.0 |
| 2403 |
Choroid plexus tumour |
1 |
Human disease
|
9.0 |
| 2404 |
Cutis laxa |
1 |
Human disease
|
11.5 |
| 2406 |
Rett syndrome, MECP2-related |
3 |
Target evidence
|
84.9 |
| 2407 |
Exercise intolerance, cytochrome B-related |
1 |
Animal disease only
|
|
| 2409 |
Vitreous degeneration |
2 |
Human disease
|
9.5 |
| 2411 |
Respiratory disease, susceptibility/resistance to |
3 |
Animal disease only
|
|
| 2412 |
Bicuspid aortic valve |
2 |
Human disease
|
12.0 |
| 2413 |
Deafness, OTOF-related |
2 |
Human disease
|
5.0 |
| 2414 |
Brucellosis, susceptibility/resistance to |
3 |
Animal disease only
|
|
| 2417 |
Laryngeal collapse, dynamic |
1 |
Animal disease only
|
|
| 2418 |
Mycotoxicosis, susceptibility/resistance to |
1 |
Animal disease only
|
|
| 2419 |
Daft lamb syndrome, Type II |
1 |
Animal disease only
|
|
| 2420 |
Sacral agenesis |
2 |
Human disease
|
12.0 |
| 2421 |
Drug metabolism, altered |
4 |
Animal disease only
|
|
| 2422 |
Occipital condylar dysplasia, asymmetrical |
1 |
Animal disease only
|
|
| 2423 |
Multiple ocular defects, WFDC1-related |
1 |
Animal disease only
|
|
| 2425 |
Ichthyosis, KRT1-related |
1 |
Human disease
|
9.0 |
| 2426 |
Coat colour, dominant spot |
1 |
Animal disease only
|
|
| 2427 |
Tuberous sclerosis, TSC1-related |
1 |
Human disease
|
5.0 |
| 2429 |
Horn fly, susceptibility/resistance to |
1 |
Animal disease only
|
|
