has material basis in germline mutation in NHLRC2 syndromic disease hereditary disease fibrosis, neurodegeneration, and cerebral angiomatosis http://github.com/monarch-initiative/mondo/issues/9142 https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/fibrosis_neurodegeneration_and_cerebral_angiomatosis Orphanet:621758 GARD:0027940 MONDO:0032651 FINCA FINCA syndrome UMLS:C4748939 OMIM:618278 MEDGEN:1648312 Any syndromic disease caused by a mutation in the NHLRC2 gene and is characterized by severe progressive cerebropulmonary symptoms, resulting in death in infancy from respiratory failure. Features include malabsorption, progressive growth failure, recurrent infections, chronic hemolytic anemia, and transient liver dysfunction. fibrosis-neurodegeneration-cerebral angiomatosis syndrome