Woodhouse–Sakati syndrome has an autosomal recessive pattern of inheritance.
Mutations in the C2ORF37 gene, located at human chromosome2q22.3-q35, are believed to be the cause of Woodhouse–Sakati syndrome. The disorder is inherited in an autosomal recessive manner. This means the defective gene responsible for the disorder is located on an autosome (chromosome 2 is an autosome), and two copies of the defective gene (one inherited from each parent) are required in order to be born with the disorder. The parents of an individual with an autosomal recessive disorder both carry one copy of the defective gene, but usually do not experience any signs or symptoms of the disorder.
^ abcMedica I, Sepcic J, Peterlin B (2007). "Woodhouse-Sakati syndrome: case report and symptoms review". Genet Couns.18 (2): 227–231. PMID17710875.
^Woodhouse NJ, Sakati NA (1983). "A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities". J. Med. Genet.20 (3): 216–9. doi:10.1136/jmg.20.3.216. PMID6876115.