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Summary Literature (0)
MIM:616373 - PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE SYNDROME, TELOMERE-RELATED, 3; PFBMFT3

Xenbase Genes: rtel1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014613 - cervical spinal cord gray matter
MONDO:0800029 - obsolete interstitial lung disease 2