has material basis in germline mutation in ALDH3A2 integumentary system disorder eye disorder autosomal recessive disease Sjogren-Larsson syndrome https://github.com/monarch-initiative/mondo/issues/6749 https://rarediseases.info.nih.gov/diseases/7654/sjogren-larsson-syndrome https://www.malacards.org/card/sjogren_larsson_syndrome UMLS:C0037231 DOID:14501 MONDO:0010031 Sjögren-Larsson syndrome SLS Senior-Løken Syndrome A neurocutaneous disorder caused by an inborn error of lipid metabolism and characterized by congenital ichthyosis, intellectual deficit, and spasticity. SCTID:111303009 MEDGEN:11443 icd11.foundation:418359090 FAO deficiency MESH:D016111 NORD:1377 GARD:0007654 Orphanet:816 NANDO:1200620 NANDO:2200994 Sjogren-Larsson syndrome OMIM:270200 fatty acid alcohol oxidoreductase deficiency FADH deficiency MedDRA:10048676 NCIT:C85070 syndromic dyslipidemia disorder of phospholipids, sphingolipids and fatty acids biosynthesis leukodystrophy