has material basis in germline mutation in FOXF1 alveolar capillary dysplasia with misalignment of pulmonary veins https://github.com/monarch-initiative/mondo/issues/5537 https://rarediseases.info.nih.gov/diseases/8644/alveolar-capillary-dysplasia https://www.malacards.org/card/alveolar_capillary_dysplasia_with_misalignment_of_pulmonary_veins https://www.malacards.org/card/persistent_fetal_circulation_syndrome alveolar capillary dysplasia with pulmonary venous misalignment alveolar capillary dysplasia with misalignment of pulmonary vessels alveolar capillary dysplasia with misalignment of pulmonary veins and other congenital anomalies persistent foetal circulation alveolar capillary dysplasia DOID:13042 NCIT:C98809 MESH:C536590 MedDRA:10054726 MONDO:0009934 GARD:0008644 Editor note: MESH and NCIT split this, see NCIT:C98809 persistent fetal circulation Orphanet:210122 MEDGEN:755478 OMIM:265380 NORD:759 SCTID:447275002 familial persistent pulmonary hypertension of the newborn congenital alveolar capillary dysplasia pulmonary hypertension, familial persistent of the newborn UMLS:C2960310 ICD9:747.83 alveolar capillary dysplasia with misalignment of pulmonary veins ACDMPV foetal circulation A rare and fatal developmental lung disease characterized by respiratory distress in neonates due to refractory hypoxemia and severe pulmonary arterial hypertension. ICD9:747.49 persistent foetal circulation syndrome primary interstitial lung disease specific to childhood congenital pulmonary veins anomaly inherited interstitial lung disease cardiogenetic disease