Disease #04605 (PFBMFT4 (fibrosis, pulmonary, and/or bone marrow failure, telomere-related, type 4 (PFBMFT-4)), OMIM:616371)

Official abbreviation PFBMFT4
Name fibrosis, pulmonary, and/or bone marrow failure, telomere-related, type 4 (PFBMFT-4)
OMIM ID 616371
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PARN
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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