interstitial lung disease pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome https://github.com/monarch-initiative/mondo/issues/6754 https://www.malacards.org/card/pulmonary_fibrosis_hepatic_hyperplasia_bone_marrow_hypoplasia_syndrome Orphanet:210136 GARD:0020449 MEDGEN:1385709 MONDO:0016214 UMLS:C4510085 Pulmonary fibrosis - hepatic hyperplasia - bone marrow hypoplasia, also named Btrimorphic syndromeB (i.e. three (inherited) morbidities, pulmonary, hepatic and cytopenia), is a rare disease reported in 4 cases to date, manifesting with idiopathic pulmonary fibrosis, hepatic nodular regenerative hyperplasia leading to portal hypertension and thrombocytopenia due to bone marrow hypoplasia. The condition was associated with 100% mortality.