All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03850 DKCB5;DCKA4 dyskeratosis congenita, autosomal recessive, type 5 (DKCB-5, autosomal dominant, type 4 (DKCA-4)) 615190 AD;AR - - RTEL1 - -
04650 PFBMFT3 fibrosis, pulmonary, and/or bone marrow failure, telomere-related, type 3 (PFBMFT-3) 616373 AD - - RTEL1 - -
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