Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4

rare

Any pulmonary fibrosis and/or bone marrow failure, Telomere-related in which the cause of the disease is a mutation in the PARN gene.

Identifiers: MONDO:0014612 OMIM:616371
Causal genes: PARN
Part of: Pulmonary fibrosis and/or bone marrow failure, telomere-related
Also known as: PARN pulmonary fibrosis and/or bone marrow failure, Telomere-related · PFBMFT4 · pulmonary fibrosis and/or bone marrow failure, Telomere-related caused by mutation in PARN · pulmonary fibrosis and/or bone marrow failure, Telomere-related, type 4

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