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Up to: Dyskeratosis congenita and related telomere biology disorder · Pulmonary fibrosis and/or bone marrow failure, telomere-related
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3
Any pulmonary fibrosis and/or bone marrow failure, Telomere-related in which the cause of the disease is a mutation in the RTEL1 gene.
This condition has no sub-types.