is a congenital heart defect where the ductus arteriosus stays open.

is a rare genetic disorder affecting the heart and hand development.

is a small hole between the heart's upper chambers present after birth.

is a birth difference where the bladder connects to the belly button.

is a rare genetic condition caused by missing paternal chromosome 20 material.

is a genetic condition where both chromosome copies come from the father.

is when both copies of chromosome 1 come from the father.

is a rare genetic condition with both chromosome 13 copies paternal.

is a rare genetic condition with both chromosome 20 copies inherited paternally.

is when both copies of chromosome 21 come from the father.

is a rare genetic condition with both chromosome 5 copies inherited paternally.

is a rare genetic condition involving two paternal copies of chromosome 6.

happens when both copies of chromosome 7 come from the father.

is a rare genetic condition caused by inheriting both X chromosomes paternally.

causes involuntary, repetitive eye movements from inner ear or brain problems.

is a behavioral addiction causing persistent, harmful gambling despite consequences.

is an inherited eye condition affecting the retina and central vision.

is an inherited eye condition affecting the macula and central vision.

is an inherited eye disorder causing patterned retinal changes and central vision problems.

is an inherited eye disorder affecting the macula and central vision.

is a rare genetic disorder affecting growth, facial features, and development.

is when the tube linking your middle ear and throat stays open.

is a kidney inflammation often linked to vasculitis that can progress rapidly.

is a rare autoimmune kidney inflammation linked to ANCA antibodies.