| 2050 |
Hypomagnesaemia, subclinical |
1 |
Human disease
|
9.0 |
| 2052 |
Hyperphosphatemia |
1 |
Human disease
|
9.0 |
| 2053 |
Hydrallantois |
5 |
Animal disease only
|
|
| 2054 |
Cancer, RUNX-related |
1 |
Animal disease only
|
|
| 2055 |
Degenerative encephalopathy, RB1CC1-related |
1 |
Animal disease only
|
|
| 2056 |
Periodontitis |
1 |
Human disease
|
9.0 |
| 2059 |
Haplotype with homozygous deficiency 8-2026 |
1 |
Animal disease only
|
|
| 2060 |
Adrenal hypoplasia, congenital |
1 |
Human disease
|
10.0 |
| 2062 |
Guillain-Barr-like polyradiculoneuropathy |
2 |
Human disease
|
32.0 |
| 2063 |
Hyperlipidaemia/atherosclerosis, APOE-related |
4 |
Human disease
|
30.0 |
| 2064 |
Autoimmune lymphoproliferative syndrome, FASLG-related |
1 |
Drug
|
56.0 |
| 2065 |
Niemann-Pick disease, type C2 |
1 |
Human disease
|
14.0 |
| 2067 |
Syndactyly, type Ia |
1 |
Human disease
|
9.0 |
| 2068 |
Dwarfism, B4GALT7-related |
1 |
Human gene
|
29.0 |
| 2069 |
Dystonia, generic |
3 |
Animal disease only
|
|
| 2070 |
Stevens-Johnson syndrome, predisposition to |
1 |
Human disease
|
34.0 |
| 2071 |
Macular corneal dystrophy |
1 |
Target evidence
|
56.4 |
| 2072 |
Myasthenic syndrome, congenital, CHAT-related |
1 |
Human gene
|
34.0 |
| 2073 |
Mannheimia haemolytica, susceptibility/resistance to |
3 |
Animal disease only
|
|
| 2075 |
Beak, crossed |
1 |
Animal disease only
|
|
| 2078 |
Tyrosinaemia, type I |
2 |
Human disease
|
15.0 |
| 2079 |
Hyperhomocysteinaemia |
1 |
Human disease
|
29.0 |
| 2080 |
Epidermolysis bullosa, simplex, PLEC-related |
1 |
Target evidence
|
56.7 |
| 2081 |
Epidermolysis bullosa simplex, KRT5-related |
3 |
Target evidence
|
61.9 |
| 2082 |
Epidermolysis bullosa, simplex |
3 |
Human disease
|
15.0 |
| 2083 |
Abortion (embryonic lethality), ANXA10-related |
1 |
Animal disease only
|
|
| 2084 |
Dyskinesia, paroxysmal, PIGN-related |
1 |
Target evidence
|
57.5 |
| 2085 |
Retinal atrophy, progressive, Whippet |
1 |
Animal disease only
|
|
| 2086 |
Degenerative suspensory ligament desmitis |
1 |
Animal disease only
|
|
| 2088 |
Palmoplantar keratoderma, nonepidermolytic, focal 1 |
1 |
Human disease
|
14.0 |
| 2089 |
Ataxia, cerebellar, KCNJ10-related |
1 |
Target evidence
|
63.3 |
| 2090 |
Facial dysplasia syndrome |
1 |
Drug
|
61.8 |
| 2091 |
Ataxia, cerebellar, generic |
3 |
Animal disease only
|
|
| 2092 |
Ataxia, spinocerebellar, SPTBN2-related |
1 |
Target evidence
|
57.0 |
| 2094 |
Aortic aneurysm, generic |
3 |
Animal disease only
|
|
| 2095 |
Epilepsy, generalized myoclonic, with photosensitivity |
1 |
Animal disease only
|
|
| 2096 |
Naked foal syndrome |
1 |
Target evidence
|
56.3 |
| 2097 |
Ataxia, spinocerebellar, ITPR1-related |
1 |
Target evidence
|
57.9 |
| 2098 |
Digital flexor musculotendinous contracture |
1 |
Animal disease only
|
|
| 2099 |
Ichthyosis, ASPRV1-related |
1 |
Human disease
|
9.0 |
| 2101 |
Oculocutaneous hypopigmentation |
2 |
Animal disease only
|
|
| 2103 |
Developmental duplications |
1 |
Animal disease only
|
|
| 2104 |
Corkscrew claw |
2 |
Animal disease only
|
|
| 2105 |
Neuroaxonal dystrophy, PLA2G6-related |
2 |
Target evidence
|
79.5 |
| 2106 |
Feather, abnormal growth |
1 |
Animal disease only
|
|
| 2109 |
Tricho-dento-osseous-like syndrome |
1 |
Target evidence
|
58.3 |
| 2110 |
Ataxia, cerebellar, ATP1B2-related |
1 |
Animal disease only
|
|
| 2111 |
Cataract, recessive, CPAMD8-related |
1 |
Human gene
|
34.0 |
| 2112 |
Osteogenesis imperfecta, COL1A2-related |
2 |
Drug
|
64.1 |
| 2113 |
Lower jaw deformity |
1 |
Animal disease only
|
|
