Disease #03719 (PFBMFT2 (fibrosis, pulmonary, and/or bone marrow failure, telomere-related, type 2 (PFBMFT-2)), OMIM:614743)

Official abbreviation PFBMFT2
Name fibrosis, pulmonary, and/or bone marrow failure, telomere-related, type 2 (PFBMFT-2)
OMIM ID 614743
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene TERC
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00105104 ? PubMed: Alder 2008 - - - - - - - - - PFBMFT2 idiopathic pulmonary fibrosis TERC TERC 1 1 Johan den Dunnen
00105108 ? PubMed: Alder 2011 - - - - - - - - - PFBMFT2 idiopathic pulmonary fibrosis TERC TERC 1 1 Johan den Dunnen
00105120 ? PubMed: Marrone 2007 - - - - - - - - - PFBMFT2 pulmonary fibrosis TERC TERC 1 1 Johan den Dunnen
00105131 ? PubMed: Armanios 2007 - - - - - - - - - PFBMFT2 idiopathic pulmonary fibrosis TERC TERC 1 1 Johan den Dunnen
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