has material basis in germline mutation in BANF1 autosomal recessive disease Nestor-Guillermo progeria syndrome https://github.com/monarch-initiative/mondo/issues/8191 https://rarediseases.info.nih.gov/diseases/11008/nestor-guillermo-progeria-syndrome https://www.malacards.org/card/nestor_guillermo_progeria_syndrome UMLS:C3151446 A premature aging syndrome, autosomal recessive, characterized by lipoatrophy, osteoporosis, and very severe osteolysis. Patients have no cardiovascular impairment, diabetes mellitus, or hypertriglyceridemia, but suffer profound skeletal abnormalities that affect their quality of life. BANF1-related neurodevelopmental syndrome progeria syndrome, childhood-onset, with osteolysis OMIM:614008 NGPS GARD:0011008 PSCOO DOID:0081334 Orphanet:280576 MEDGEN:462796 Nestor-Guillermo progeria syndrome MONDO:0013523 progeroid syndrome primary osteolysis