is a rare genetic condition causing fused or webbed fingers and toes.

is a rare inherited condition causing fusion of certain fingers.

is a genetic condition causing fused digits, bent pinkies, and split toes.

is a rare genetic condition causing joined digits and involuntary eye movements.

is a genetic condition causing fused or extra digits and ear changes.

is a rare genetic syndrome causing fused digits and multiple birth defects.

is a genetic condition linked to an enlarged, weakened heart muscle.

is a genetic syndrome linked to thickened heart muscle and related complications.

is a rare genetic condition causing poor response to thyroid hormone.

is a rare condition causing abnormalities of the head and neck.

is a condition where XX chromosomes are linked with atypical sex development.

is a sex development condition affecting some people with 46,XY chromosomes.

is a genetic condition marked by major brain or spinal cord malformations.

is a genetic syndrome marked by cerebellar changes and related developmental problems.

is a genetic syndrome often involving Dandy-Walker brain malformation and developmental differences.

is a rare genetic disorder affecting development, learning, and blood cells.

is a rare immune disorder causing frequent infections and other health problems.

is a rare condition with a partly or fully missing corpus callosum.

is a difference in sex development affecting reproductive anatomy and hormones.

is a genetic condition causing low calcium from underactive parathyroid glands.

is a rare genetic condition causing extra, fused, or duplicated digits.

is a genetic condition mainly affecting limb development and body growth.

is a genetic condition involving missing or underdeveloped limbs and other features.

is a genetic condition causing a small head and developmental differences.