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小組
Usher 綜合征
Usher 綜合征
發(fā)起討論
Usher 綜合征
13 個(gè)討論
只看精華帖
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通常USH2A沒有前庭障礙，但我是個(gè)例外
多情的20號染色體
? 最后回復(fù)
爽朗的9號染色體
?
2024-12-03 09:52
525
1
? 來自相關(guān)小組
RS397518039是什么點(diǎn)位啊
hulihuli
? 最后回復(fù)
帥呆的PSAT1基因
?
2024-12-03 02:59
914
1
? 來自相關(guān)小組
Usher綜合癥
看海的CELF2基因
? 最后回復(fù)
WeGene_9EC5DDE2
?
2024-10-04 15:55
765
3
? 來自相關(guān)小組
chr1:215844567是什么位點(diǎn)？
xuebowen021
? 最后回復(fù)
唏噓的8號染色體
?
2021-11-28 12:19
3005
1
? 來自相關(guān)小組
我天生夜盲，耳朵對低音講話的人辨識度有點(diǎn)差。。
熱血豆腐
? 最后回復(fù)
xuebowen021
?
2021-11-28 06:07
3021
2
? 來自相關(guān)小組
攜帶usher綜合征基因
咆哮的GCFC2基因
? 最后回復(fù)
zhengqiang
?
2021-04-08 00:41
2395
1
? 來自相關(guān)小組
求助，夫妻雙方都是usher綜合癥風(fēng)險(xiǎn)變異攜帶者，產(chǎn)前怎么辦？
養(yǎng)貓的17號染色體
? 最后回復(fù)
AileenJS
?
2019-06-04 23:06
5297
6
? 來自相關(guān)小組
我是不是別找也攜帶的人生孩子就風(fēng)險(xiǎn)不大？
狗醬醬
? 最后回復(fù)
mabaoyuan037
?
2019-03-13 18:45
2967
2
? 來自相關(guān)小組
這個(gè)是隱性疾病，有攜帶是不是沒關(guān)系??？
Jamie杰
? 最后回復(fù)
虛心的GOT2基因
?
2018-12-27 16:46
3206
1
? 來自相關(guān)小組
攜帶一個(gè)基因間突變
摩羯的RXRA基因
? 2018-12-16 07:29
3031
0
? 來自相關(guān)小組
有這個(gè)是不是不要小孩比較好啊
俊逸的MLH1基因
? 最后回復(fù)
俊逸的MLH1基因
?
2018-12-13 21:25
3366
3
? 來自相關(guān)小組
這是啥？需不需要去醫(yī)院查查啊
傷情的DSCAM基因
? 最后回復(fù)
hahadada
?
2018-12-12 19:36
3327
3
? 來自相關(guān)小組
臥槽 我確實(shí)感覺自己耳背
黑豆?jié){2333
? 最后回復(fù)
元月十號
?
2018-12-09 11:12
3136
1
? 來自相關(guān)小組
發(fā)起討論
Usher 綜合征
13 個(gè)討論
相關(guān)基因
MYO7A
位點(diǎn)：RS111033174
位點(diǎn)：RS111033178
位點(diǎn)：RS111033180
位點(diǎn)：RS111033181
位點(diǎn)：RS111033182
位點(diǎn)：RS111033192
位點(diǎn)：RS111033198
位點(diǎn)：RS111033201
位點(diǎn)：RS111033206
位點(diǎn)：RS111033214
位點(diǎn)：RS111033233
位點(diǎn)：RS111033283
位點(diǎn)：RS111033285
位點(diǎn)：RS111033290
位點(diǎn)：RS111033389
位點(diǎn)：RS111033426
位點(diǎn)：RS111033482
位點(diǎn)：RS121965079
位點(diǎn)：RS121965085
位點(diǎn)：RS199606180
位點(diǎn)：RS28934610
位點(diǎn)：RS35689081
位點(diǎn)：RS397516281
位點(diǎn)：RS397516283
位點(diǎn)：RS397516284
位點(diǎn)：RS397516291
位點(diǎn)：RS397516295
位點(diǎn)：RS397516301
位點(diǎn)：RS397516310
位點(diǎn)：RS397516312
位點(diǎn)：RS397516315
位點(diǎn)：RS397516317
位點(diǎn)：RS397516320
位點(diǎn)：RS397516321
位點(diǎn)：RS397516322
位點(diǎn)：RS397516323
位點(diǎn)：RS397516324
位點(diǎn)：RS397516331
位點(diǎn)：RS397516332
位點(diǎn)：RS41298133
位點(diǎn)：RS797044518
位點(diǎn)：RS782252317
位點(diǎn)：RS781811444
位點(diǎn)：RS797044491
位點(diǎn)：RS797044511
位點(diǎn)：RS201892914
位點(diǎn)：RS781988557
位點(diǎn)：RS376535635
位點(diǎn)：RS199897298
位點(diǎn)：RS117966637
位點(diǎn)：RS369458838
位點(diǎn)：RS727503329
位點(diǎn)：RS397516316
位點(diǎn)：RS727504541
位點(diǎn)：RS111033215
位點(diǎn)：RS773844428
位點(diǎn)：RS377670513
位點(diǎn)：RS878853236
位點(diǎn)：RS878864531
CLRN1
位點(diǎn)：RS111033258
位點(diǎn)：RS111033267
位點(diǎn)：RS111033434
位點(diǎn)：RS121908140
位點(diǎn)：RS121908141
位點(diǎn)：RS121908143
位點(diǎn)：RS374963432
位點(diǎn)：RS201008540
PCDH15
位點(diǎn)：RS111033260
位點(diǎn)：RS137853001
位點(diǎn)：RS202033121
位點(diǎn)：RS397517452
位點(diǎn)：RS727504301
USH2A
位點(diǎn)：RS111033264
位點(diǎn)：RS111033265
位點(diǎn)：RS111033272
位點(diǎn)：RS111033273
位點(diǎn)：RS111033334
位點(diǎn)：RS111033364
位點(diǎn)：RS111033382
位點(diǎn)：RS111033385
位點(diǎn)：RS111033414
位點(diǎn)：RS111033417
位點(diǎn)：RS111033418
位點(diǎn)：RS111033526
位點(diǎn)：RS121912599
位點(diǎn)：RS121912600
位點(diǎn)：RS202175091
位點(diǎn)：RS369522997
位點(diǎn)：RS397517974
位點(diǎn)：RS397517976
位點(diǎn)：RS397517977
位點(diǎn)：RS397517979
位點(diǎn)：RS397517988
位點(diǎn)：RS397517989
位點(diǎn)：RS397517990
位點(diǎn)：RS397517994
位點(diǎn)：RS397518021
位點(diǎn)：RS397518022
位點(diǎn)：RS397518023
位點(diǎn)：RS397518026
位點(diǎn)：RS397518029
位點(diǎn)：RS397518036
位點(diǎn)：RS397518041
位點(diǎn)：RS397518042
位點(diǎn)：RS397518046
位點(diǎn)：RS397518048
位點(diǎn)：RS398124619
位點(diǎn)：RS41308425
位點(diǎn)：RS483353056
位點(diǎn)：RS527236137
位點(diǎn)：RS527236139
位點(diǎn)：RS80338904
位點(diǎn)：RS146733615
位點(diǎn)：RS727504867
位點(diǎn)：RS753330544
位點(diǎn)：RS201238640
位點(diǎn)：RS727505337
位點(diǎn)：RS727504608
位點(diǎn)：RS372347027
位點(diǎn)：RS201657446
位點(diǎn)：RS794727579
位點(diǎn)：RS727503725
位點(diǎn)：RS727503731
位點(diǎn)：RS797045113
位點(diǎn)：RS794729204
位點(diǎn)：RS727503736
位點(diǎn)：RS397517963
位點(diǎn)：RS111033280
位點(diǎn)：W01216380743
CDH23
位點(diǎn)：RS111033270
位點(diǎn)：RS183431253
位點(diǎn)：RS367928692
位點(diǎn)：RS370983472
位點(diǎn)：RS397517323
位點(diǎn)：RS397517326
位點(diǎn)：RS397517327
位點(diǎn)：RS397517329
位點(diǎn)：RS397517337
位點(diǎn)：RS397517341
位點(diǎn)：RS397517342
位點(diǎn)：RS397517346
位點(diǎn)：RS397517353
位點(diǎn)：RS397517354
位點(diǎn)：RS397517362
位點(diǎn)：RS727502931
位點(diǎn)：RS140884994
USH1C
位點(diǎn)：RS121908370
位點(diǎn)：RS151045328
位點(diǎn)：RS138138689
位點(diǎn)：RS377145777
ADGRV1
位點(diǎn)：RS121909762
位點(diǎn)：RS371981035
位點(diǎn)：RS373780305
位點(diǎn)：RS397517436
USH1G
位點(diǎn)：RS397517925
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 8
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 7
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 9
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 5
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 10
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.
Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 4
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 6
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
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深圳市市場監(jiān)督管理局企業(yè)主體身份公示
|
粵ICP備15012185號
| 互聯(lián)網(wǎng)藥品信息服務(wù)資格證書:（粵）-非經(jīng)營性-2023-0379
中文
English
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主站蜘蛛池模板：
安远县
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达日县
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珠海市
|
白水县
|
攀枝花市
|
长子县
|
大丰市
|
义乌市
|
上高县
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乐安县
|
准格尔旗
|
安顺市
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峡江县
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大关县
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临澧县
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合川市
|
哈巴河县
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甘南县
|
奉化市
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青神县
|
叶城县
|
上栗县
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隆回县
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巴林右旗
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五常市
|
合肥市
|
历史
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阿坝县
|
太康县
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海淀区
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察哈
|
大悟县
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抚宁县
|
东乡县
|
乌兰县
|
渭南市
|
文山县
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德庆县
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全椒县
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济阳县
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呼伦贝尔市
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深圳市市場監(jiān)督管理局企業(yè)主體身份公示
|
粵ICP備15012185號
|
互聯(lián)網(wǎng)藥品信息服務(wù)資格證書:（粵）-非經(jīng)營性-2023-0379
中文 
English
純合片段分析
姓氏祖源
祖源平均臉
基因關(guān)系
基因保險(xiǎn)助手
原始數(shù)據(jù)
