Ectopia lentis 2, isolated, autosomal recessive

An isolated ectopia lentis that has material basis in homozygous or compound heterozygous mutation in the ADAMTSL4 gene on chromosome 1q21.

Also known as: ECTOL2, ectopia lentis 2, isolated, autosomal recessive, ectopia lentis, isolated, autosomal recessive, autosomal recessive isolated ectopia lentis, autosomal recessive isolated ectopia lentis 2, ectopia lentis, isolated autosomal recessive

1 clinical trial for this condition and its sub-types, 0 tagged with Ectopia lentis 2, isolated, autosomal recessive itself.