| 2307 |
Frontonasal dysplasia, ZIC2-related |
1 |
Target evidence
|
57.6 |
| 2308 |
Cardiomyopathy, X-linked dilated |
1 |
Drug
|
59.0 |
| 2309 |
Cataract, MIP-related |
1 |
Human gene
|
29.0 |
| 2310 |
60,XX/90,XXY sex chromosome difference of sexual development |
1 |
Animal disease only
|
|
| 2311 |
Sterile, male, NANOS2-related |
4 |
Animal disease only
|
|
| 2312 |
Sterile, female, DDX4-related |
1 |
Animal disease only
|
|
| 2313 |
Cervicothoracic vertebral subluxation |
1 |
Animal disease only
|
|
| 2314 |
Pituitary hormone deficiency, LHX3-related |
1 |
Target evidence
|
56.5 |
| 2315 |
Pituitary hormone deficiency, POU1F1-related |
1 |
Target evidence
|
62.8 |
| 2316 |
Cardiomyopathy, hypertrophic, ALMS1-related |
1 |
Target evidence
|
75.3 |
| 2317 |
Abnormal gait, retinal dysplasia, cataracts, RORB-related |
1 |
Animal disease only
|
|
| 2320 |
Retinal atrophy, progressive, IFT122-related |
1 |
Human gene
|
29.0 |
| 2321 |
Leukodystrophy, hypomyelinating |
1 |
Human disease
|
6.5 |
| 2322 |
Dyskinesia, paroxysmal, SOD1-related |
1 |
Human gene
|
29.0 |
| 2323 |
Operculum, lack of |
1 |
Animal disease only
|
|
| 2324 |
Epilepsy, mitochondrial dysfunction and neurodegeneration, PITRM1-related |
1 |
Animal disease only
|
|
| 2325 |
Encephalopathy, ASPA-related |
1 |
Target evidence
|
73.9 |
| 2326 |
Deafness, KLF7-related |
1 |
Animal disease only
|
|
| 2328 |
Behaviour |
43 |
Animal disease only
|
|
| 2329 |
Hypercholesterolaemia, PCSK9-related |
2 |
Human disease
|
5.0 |
| 2330 |
Myopathy, myofibrillar |
1 |
Human disease
|
9.0 |
| 2331 |
Cardiomyopathy, TNNI3-related |
2 |
Human disease
|
9.0 |
| 2332 |
Long QT syndrome, KCNQ1-related |
2 |
Drug
|
69.3 |
| 2333 |
Long QT syndrome, KCNH2-related |
1 |
Human gene
|
29.0 |
| 2334 |
Long QT syndrome, KCNE1-related |
1 |
Target evidence
|
57.0 |
| 2335 |
Prostate cancer |
1 |
Human disease
|
31.5 |
| 2336 |
Deafness, LOXHD1-related |
1 |
Human disease
|
9.0 |
| 2337 |
Haplotype with homozygous deficiency, LDHH1 |
1 |
Animal disease only
|
|
| 2338 |
Haplotype with homozygous deficiency, LDHH2 |
1 |
Animal disease only
|
|
| 2339 |
Haplotype with homozygous deficiency, LDHH3 |
1 |
Animal disease only
|
|
| 2340 |
Haplotype with homozygous deficiency, LDHH4 |
1 |
Animal disease only
|
|
| 2341 |
Haplotype with homozygous deficiency, LDHH5 |
1 |
Animal disease only
|
|
| 2342 |
Ciliary dyskinesia, primary, CCDC65-related |
1 |
Human gene
|
29.0 |
| 2343 |
Haplotype with homozygous deficiency, LDHH7 |
1 |
Animal disease only
|
|
| 2344 |
Haplotype with homozygous deficiency, LDHH8 |
1 |
Animal disease only
|
|
| 2345 |
Haplotype with homozygous deficiency, LDHH9 |
1 |
Animal disease only
|
|
| 2346 |
Haplotype with homozygous deficiency, LDHH10 |
1 |
Animal disease only
|
|
| 2347 |
Haplotype with homozygous deficiency, LDHH11 |
1 |
Animal disease only
|
|
| 2348 |
Retinal dysplasia, NDP-related |
1 |
Human disease
|
9.0 |
| 2351 |
Transmission ratio distortion |
4 |
Animal disease only
|
|
| 2353 |
Limb movement, synchronic, EFNB3-related |
6 |
Animal disease only
|
|
| 2354 |
Male subfertility |
8 |
Animal disease only
|
|
| 2355 |
Prostatic hyperplasia, benign |
1 |
Human disease
|
34.0 |
| 2357 |
Transmissible gastroenteritis virus (TGEV), susceptibility/resistance to |
1 |
Animal disease only
|
|
| 2358 |
Porcine epidemic diarrhea virus (PEDV), susceptibility/resistance to |
1 |
Animal disease only
|
|
| 2359 |
Classical swine fever virus (CSFV), susceptibility/resistance to |
1 |
Animal disease only
|
|
| 2360 |
Deafness, OSBPL2-related |
1 |
Human disease
|
5.0 |
| 2361 |
Parkinson disease, PINK1-related |
3 |
Human gene
|
29.0 |
| 2363 |
Skin colour, white and iridophoroma |
1 |
Animal disease only
|
|
| 2364 |
Rickets, generic |
3 |
Animal disease only
|
|
