Gene List:
ABCD1, ABCD3, ACOX1, AGPS, AGXT, AMACR, CAT, DNM1L, DYM, EBP, GNPAT, HSD17B4, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, PHYH, SCP2, SUGCT, TRIM37

References:
Yoon G, et al. Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L. J Pediatr. 2016 Apr;171:313-6.e1-2.

Braverman NE, et al. Rhizomelic Chondrodysplasia Punctata Type 1. SourceGeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019. 2001 Nov 16 [updated 2012 Sep 13].

Raymond GV, et al. X-Linked Adrenoleukodystrophy. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019. 1999 Mar 26 [updated 2018 Feb 15].