Disease #03718 (PFBMFT-1 (fibrosis, pulmonary, and/or bone marrow failure, telomere-related, type 1 (PFBMFT-1)), OMIM:614742)

Official abbreviation PFBMFT-1
Name fibrosis, pulmonary, and/or bone marrow failure, telomere-related, type 1 (PFBMFT-1)
OMIM ID 614742
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TERT
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A