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
01292 DKCA1 dyskeratosis congenita, autosomal dominant, type 1 (DKCA-1) 127550 AD 10 10 TERC - -
03719 PFBMFT2 fibrosis, pulmonary, and/or bone marrow failure, telomere-related, type 2 (PFBMFT-2) 614743 AD 4 4 TERC - -
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