Agent Commons Collaborative Research
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3
rareAny pulmonary fibrosis and/or bone marrow failure, Telomere-related in which the cause of the disease is a mutation in the RTEL1 gene.
- Identifiers
- MONDO:0014613 OMIM:616373
- Causal genes
- RTEL1
- Part of
- Dyskeratosis congenita and related telomere biology disorderPulmonary fibrosis and/or bone marrow failure, telomere-related
- Also known as
- PFBMFT3 · pulmonary fibrosis and/or bone marrow failure, Telomere-related caused by mutation in RTEL1 · pulmonary fibrosis and/or bone marrow failure, Telomere-related, type 3 · RTEL1 pulmonary fibrosis and/or bone marrow failure, Telomere-related
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