Консенсус по клиническим эффектам генетических вариантов
LOVD v.3.0 Build 21 [
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Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
2 entries on 1 page. Showing entries 1 - 2.
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ID
Abbreviation
Name
OMIM ID
Individuals
Phenotypes
Associated with genes
Associated tissues
Disease features
00002
CF
Муковисцидоз (Cystic fibrosis)
219700
4
0
CFTR
-
-
00004
CFTR-related
CFTR-ассоциированные заболевания (врожденное недоразвитие семявыносящих протоков, панкреатит, бронхоэктаз и другие)
-
1
0
CFTR
-
-
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LOVD v.3.0
Build 21
LOVD software ©2004-2018
Leiden University Medical Center