DOID:0080599
|
Coronavirus infectious disease
|
MGI:95294
|
Mus musculus (house mouse)
|
13649
|
Egfr
|
|
author statement supported by traceable reference
|
|
DOID:0050466
|
Loeys-Dietz syndrome
|
MGI:98728
|
Mus musculus (house mouse)
|
21812
|
Tgfbr1
|
|
author statement supported by traceable reference
|
|
DOID:0050651
|
atrioventricular septal defect
|
MGI:1921272
|
Mus musculus (house mouse)
|
74022
|
Glyr1
|
|
author statement supported by traceable reference
|
|
DOID:0050766
|
choreaacanthocytosis
|
MGI:2444304
|
Mus musculus (house mouse)
|
271564
|
Vps13a
|
|
author statement supported by traceable reference
|
|
DOID:0110594
|
primary ciliary dyskinesia 1
|
MGI:1916172
|
Mus musculus (house mouse)
|
68922
|
Dnai1
|
|
author statement supported by traceable reference
|
- MGI:5284969
- PMID:19675306
|
DOID:13628
|
favism
|
MGI:105979
|
Mus musculus (house mouse)
|
14381
|
G6pdx
|
|
author statement supported by traceable reference
|
- PMID:12777375
- PMID:14751857
- PMID:3377761
|
DOID:9452
|
steatotic liver disease
|
MGI:104663
|
Mus musculus (house mouse)
|
16846
|
Lep
|
|
author statement supported by traceable reference
|
|
DOID:0060850
|
annular pancreas
|
MGI:96533
|
Mus musculus (house mouse)
|
16147
|
Ihh
|
|
author statement supported by traceable reference
|
|
DOID:0060041
|
autism spectrum disorder
|
MGI:87891
|
Mus musculus (house mouse)
|
11444
|
Chrnb2
|
|
author statement supported by traceable reference
|
|
DOID:3827
|
congenital diaphragmatic hernia
|
MGI:1352452
|
Mus musculus (house mouse)
|
11819
|
Nr2f2
|
|
author statement supported by traceable reference
|
|
DOID:12347
|
osteogenesis imperfecta
|
MGI:88467
|
Mus musculus (house mouse)
|
12842
|
Col1a1
|
|
author statement supported by traceable reference
|
|
DOID:0060041
|
autism spectrum disorder
|
MGI:1914047
|
Mus musculus (house mouse)
|
66797
|
Cntnap2
|
|
author statement supported by traceable reference
|
- PMID:21962519
- PMID:26647347
|
DOID:0110199
|
Charcot-Marie-Tooth disease dominant intermediate C
|
MGI:2147627
|
Mus musculus (house mouse)
|
107271
|
Yars1
|
|
author statement supported by traceable reference
|
|
DOID:0060041
|
autism spectrum disorder
|
MGI:2444609
|
Mus musculus (house mouse)
|
245537
|
Nlgn3
|
|
author statement supported by traceable reference
|
- PMID:17823315
- PMID:19243448
- PMID:22983708
- PMID:24995986
|
DOID:0050477
|
Liddle syndrome
|
MGI:104696
|
Mus musculus (house mouse)
|
20277
|
Scnn1b
|
|
author statement supported by traceable reference
|
|
DOID:0050557
|
congenital muscular dystrophy
|
MGI:88461
|
Mus musculus (house mouse)
|
12835
|
Col6a3
|
|
author statement supported by traceable reference
|
|
DOID:12798
|
mucopolysaccharidosis
|
MGI:1921258
|
Mus musculus (house mouse)
|
74008
|
Arsg
|
|
author statement supported by traceable reference
|
|
DOID:0110291
|
Leber congenital amaurosis 10
|
MGI:2384917
|
Mus musculus (house mouse)
|
216274
|
Cep290
|
|
author statement supported by traceable reference
|
- PMID:17898177
- PMID:21245082
|
DOID:0050770
|
polycystic liver disease
|
MGI:107877
|
Mus musculus (house mouse)
|
19089
|
Prkcsh
|
|
author statement supported by traceable reference
|
|
DOID:2750
|
glycogen storage disease IV
|
MGI:1921435
|
Mus musculus (house mouse)
|
74185
|
Gbe1
|
|
author statement supported by traceable reference
|
- PMID:21075835
- PMID:21856731
- PMID:26385640
|
DOID:0060843
|
hereditary neuropathy with liability to pressure palsies
|
MGI:97631
|
Mus musculus (house mouse)
|
18858
|
Pmp22
|
|
author statement supported by traceable reference
|
- MGI:5515889
- PMID:16436605
- PMID:7581450
|
DOID:1612
|
breast cancer
|
MGI:95410
|
Mus musculus (house mouse)
|
13866
|
Erbb2
|
|
author statement supported by traceable reference
|
- PMID:18273058
- PMID:20961995
|
DOID:2377
|
multiple sclerosis
|
MGI:97551
|
Mus musculus (house mouse)
|
18646
|
Prf1
|
|
author statement supported by traceable reference
|
|
DOID:0050580
|
hereditary lymphedema
|
MGI:109124
|
Mus musculus (house mouse)
|
22341
|
Vegfc
|
|
author statement supported by traceable reference
|
|
DOID:0110552
|
autosomal dominant nonsyndromic deafness 22
|
MGI:104785
|
Mus musculus (house mouse)
|
17920
|
Myo6
|
|
author statement supported by traceable reference
|
- PMID:31103816
- PMID:7493015
|