has material basis in germline mutation in TRIM37 syndromic disease autosomal recessive disease mulibrey nanism https://github.com/monarch-initiative/mondo/issues/2632 https://rarediseases.info.nih.gov/diseases/95/mulibrey-nanism https://www.malacards.org/card/mulibrey_nanism MONDO:0009664 GARD:0000095 NCIT:C84906 mulibrey dwarfism ICD9:759.89 muscle-liver-brain-eye nanism OMIM:253250 SCTID:81604003 MESH:D050336 Orphanet:2576 pericardial constriction-growth failure syndrome MUL icd11.foundation:1167260635 DOID:0050436 pericardial constriction and growth failure MEDGEN:99347 A prenatal onset growth disorder with multiorgan manifestations. NORD:1465 mulibrey nanism Perheentupa syndrome UMLS:C0524582 disorder of development or morphogenesis disorder of defective peroxisome oxidative status