Sjogren-Larsson syndrome

Summary
Synonym
  • FALDH deficiency
  • SLS
  • Sjogren Larsson syndrome
  • Sjogren-Larsson's syndrome
  • fatty acid alcohol oxidoreductase deficiency
Definition
A syndrome that is characterized by ichthyosis, mental retardation, spastic paraparesis, macular dystrophy, and leukoencephalopathy, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the aldehyde dehydrogenase 3 family member A2 (ALDH3A2) gene, which encodes fatty aldehyde dehydrogenase, on chromosome 17p11.
Super Class
autosomal recessive disease syndrome
External Links
Disease Ontology
DOID:14501
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 1 - 10 of 17 in total
Gene ID Gene Symbol Description Source
128 ADH5 alcohol dehydrogenase 5 (class III), chi polypeptide
218 ALDH3A1 aldehyde dehydrogenase 3 family member A1
221 ALDH3B1 aldehyde dehydrogenase 3 family member B1
222 ALDH3B2 aldehyde dehydrogenase 3 family member B2
224 ALDH3A2 aldehyde dehydrogenase 3 family member A2
242 ALOX12B arachidonate 12-lipoxygenase, 12R type
412 STS steroid sulfatase
2181 ACSL3 acyl-CoA synthetase long chain family member 3
2182 ACSL4 acyl-CoA synthetase long chain family member 4
2629 GBA1 glucosylceramidase beta 1
Related Glycoprotein
Displaying entry 11 - 11 of 11 in total
UniProt ID Protein Name Source
Q9GZR5 Very long chain fatty acid elongase 4
The Human Phenotype Ontology
Displaying entries 11 - 20 of 42 in total
HPO ID HPO Term
HP:0000682 Abnormal dental enamel morphology
HP:0010783 Erythema
HP:0001249 Intellectual disability
HP:0002650 Scoliosis
HP:0000252 Microcephaly
HP:0001257 Spasticity
HP:0004322 Short stature
HP:0000613 Photophobia
HP:0008064 Ichthyosis
HP:0001025 Urticaria
Displaying 1 entry
Gene ID Gene Symbol Description
224 ALDH3A2 aldehyde dehydrogenase 3 family member A2

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Last updated: August 19, 2024