All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03523 DFNB29 deafness, autosomal recessive, type 29 (DFNB-29) 614035 AR - - CLDN14 - -
05641 HELIX HELIX syndrome (HELIX) 617671 AR - - CLDN10 - -
01903 HOMG3 hypomagnesemia, type 3, renal (HOMG-3) 248250 AR 1 1 CLDN16 - -
01902 HOMG5 hypomagnesemia, type 5, renal, with ocular involvement (HOMG-5) 248190 AR - - CLDN19 - -
02681 ILVASC Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis 607626 AR - - CLDN1 - -
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