Albinism is an autosomal recessive disorder. This means that a person must inherit two copies of the nonfunctional gene, one from each parent, to manifest the condition. In autosomal recessive disorders, individuals with one normal allele and one defective allele are carriers, and they do not show symptoms of the disorder.
Here's a brief comparison to clarify:
Disorder
Inheritance Pattern
Albinism
Autosomal Recessive
Huntington’s Syndrome
Autosomal Dominant
Marfan’s Syndrome
Autosomal Dominant
Neurofibromatosis-1
Autosomal Dominant
Albinism results from the lack of melanin production due to enzyme deficiencies involving the biosynthesis pathway of melanin. The clinical manifestations of albinism include ocular problems, such as nystagmus and photophobia, along with visual anomalies, all deriving from the lack of pigmentation affecting eye development.