Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3

MONDO:0014613

Any pulmonary fibrosis and/or bone marrow failure, Telomere-related in which the cause of the disease is a mutation in the RTEL1 gene.

Also known as: RTEL1 pulmonary fibrosis and/or bone marrow failure, Telomere-related, pulmonary fibrosis and/or bone marrow failure, Telomere-related caused by mutation in RTEL1, pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3, pulmonary fibrosis and/or bone marrow failure, Telomere-related, type 3, PFBMFT3, pulmonary fibrosis and/or bone marrow failure, TELOMERE-RELATED, 3

100 clinical trials for this condition and its sub-types, 0 tagged with Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3 itself.

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↑ Dyskeratosis congenita and related telomere biology disorder (1) ↑ Pulmonary fibrosis and/or bone marrow failure, telomere-related (1)

Including sub-types (100) Tagged with Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3 (0)

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