All diseases associated with gene KCNJ1

11 entries on 1 page. Showing entries 1 - 11.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated tissues

Disease features
00863 - SESAME syndrome 612780 - - - - -
00864 - Enlarged vestibular aqueduct, digenic 600791 - - - - -
02394 - Islet cell hyperplasia 601820 - - - - -
02959 - Transient neonatal diabetes mellitus 3 610582 - - - - -
00965 Bartter-2 Bartter syndrome, type 2 241200 - - - - -
00139 ID intellectual disability (ID) - - - - - -
03573 LCA-16 Leber congenital amaurosis, type 16 (LCA-16) 614186 - - - - -
04542 MODY-13 diabetes of the young, maturity-onset, type 13 (MODY-13) 616329 - - - - -
00151 NIDDM diabetes mellitus, noninsulin-dependent (NIDDM) 125853 - - - - -
02098 PDS Pendred syndrome (PDS) 274600 - - - - -
01601 SVD vitreoretinal degeneration, snwoflake type (SVD) 193230 - - - - -
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