|
DOID:12583
|
velocardiofacial syndrome
|
MGI:105923
|
Mus musculus (house mouse)
|
13617
|
Ednra
|
|
author statement supported by traceable reference
|
|
|
DOID:9164
|
achalasia
|
MGI:96794
|
Mus musculus (house mouse)
|
16905
|
Lmna
|
|
author statement supported by traceable reference
|
|
|
DOID:0080720
|
autosomal dominant congenital deafness with onychodystrophy
|
MGI:109618
|
Mus musculus (house mouse)
|
11966
|
Atp6v1b2
|
|
author statement supported by traceable reference
|
|
|
DOID:11721
|
glycogen storage disease VII
|
MGI:97548
|
Mus musculus (house mouse)
|
18642
|
Pfkm
|
|
author statement supported by traceable reference
|
|
|
DOID:0050545
|
visceral heterotaxy
|
MGI:97515
|
Mus musculus (house mouse)
|
18552
|
Pcsk5
|
|
author statement supported by traceable reference
|
|
|
DOID:0050431
|
arrhythmogenic right ventricular cardiomyopathy
|
MGI:1196466
|
Mus musculus (house mouse)
|
13511
|
Dsg2
|
|
author statement supported by traceable reference
|
|
|
DOID:9074
|
systemic lupus erythematosus
|
MGI:88337
|
Mus musculus (house mouse)
|
21947
|
Cd40lg
|
|
author statement supported by traceable reference
|
|
|
DOID:1909
|
melanoma
|
MGI:88190
|
Mus musculus (house mouse)
|
109880
|
Braf
|
|
author statement supported by traceable reference
|
|
|
DOID:14330
|
Parkinson's disease
|
MGI:1921494
|
Mus musculus (house mouse)
|
74244
|
Atg7
|
|
author statement supported by traceable reference
|
|
|
DOID:5419
|
schizophrenia
|
MGI:94862
|
Mus musculus (house mouse)
|
13162
|
Slc6a3
|
|
author statement supported by traceable reference
|
|
|
DOID:0110381
|
retinitis pigmentosa 14
|
MGI:109571
|
Mus musculus (house mouse)
|
22157
|
Tulp1
|
|
author statement supported by traceable reference
|
|
|
DOID:0111030
|
hemochromatosis type 3
|
MGI:1354956
|
Mus musculus (house mouse)
|
50765
|
Tfr2
|
|
author statement supported by traceable reference
|
- PMID:12134060
- PMID:20179178
|
|
DOID:0050790
|
fibular hypoplasia and complex brachydactyly
|
MGI:95688
|
Mus musculus (house mouse)
|
14563
|
Gdf5
|
|
author statement supported by traceable reference
|
|
|
DOID:0050548
|
hereditary sensory neuropathy
|
MGI:1345149
|
Mus musculus (house mouse)
|
24046
|
Scn11a
|
|
author statement supported by traceable reference
|
|
|
DOID:0060929
|
non-syndromic X-linked intellectual developmental disorder 111
|
MGI:2679449
|
Mus musculus (house mouse)
|
245450
|
Slitrk2
|
|
author statement supported by traceable reference
|
|
|
DOID:1826
|
epilepsy
|
MGI:2441982
|
Mus musculus (house mouse)
|
214579
|
Aldh5a1
|
|
author statement supported by traceable reference
|
|
|
DOID:0060648
|
anterior segment dysgenesis
|
MGI:1929183
|
Mus musculus (house mouse)
|
64930
|
Tsc1
|
|
author statement supported by traceable reference
|
|
|
DOID:0050548
|
hereditary sensory neuropathy
|
MGI:104627
|
Mus musculus (house mouse)
|
13518
|
Dst
|
|
author statement supported by traceable reference
|
|
|
DOID:11476
|
osteoporosis
|
MGI:109587
|
Mus musculus (house mouse)
|
18383
|
Tnfrsf11b
|
|
author statement supported by traceable reference
|
|
|
DOID:9970
|
obesity
|
MGI:101932
|
Mus musculus (house mouse)
|
12876
|
Cpe
|
|
author statement supported by traceable reference
|
|
|
DOID:446
|
primary hyperaldosteronism
|
MGI:94924
|
Mus musculus (house mouse)
|
13489
|
Drd2
|
|
author statement supported by traceable reference
|
|
|
DOID:4154
|
dentinogenesis imperfecta
|
MGI:109172
|
Mus musculus (house mouse)
|
666279
|
Dspp
|
|
author statement supported by traceable reference
|
|
|
DOID:12930
|
dilated cardiomyopathy
|
MGI:1352452
|
Mus musculus (house mouse)
|
11819
|
Nr2f2
|
|
author statement supported by traceable reference
|
|
|
DOID:0060445
|
congenital stromal corneal dystrophy
|
MGI:94872
|
Mus musculus (house mouse)
|
13179
|
Dcn
|
|
author statement supported by traceable reference
|
|
|
DOID:3413
|
alpha-mannosidosis
|
MGI:107286
|
Mus musculus (house mouse)
|
17159
|
Man2b1
|
|
author statement supported by traceable reference
|
- PMID:10400983
- PMID:16014715
|