is a rare genetic disorder causing weak bones, fractures, and dental problems.

is a low blood phosphate level that can affect muscles and bones.

is a disorder causing low phosphate, kidney stones, and weak bones.

is a rare genetic disorder causing phosphate wasting, kidney stones, and osteoporosis.

is a genetic disorder causing low phosphate, kidney stones, and osteoporosis.

is usually a genetic disorder causing low phosphate, weak bones, growth problems.

causes lighter-colored eyelid skin, often from reduced melanin or inflammation.

is a condition causing lighter patches or areas of skin.

is a rare genetic skin disorder causing palm/sole thickening and light patches.

is a rare heart defect affecting the ring around the mitral valve.

is a rare genetic disorder causing low plasminogen and impaired clot breakdown.

is an inherited condition causing unusually thin, hard outer tooth enamel.

is a congenital (present at birth) heart defect with underdeveloped left chambers.

is a rare genetic disorder causing underdeveloped digestive organs and intestinal blockage.

is a rare congenital heart defect affecting the right side’s development.

is a layer of white blood cells pooled in the eye.

is a serious corneal infection causing a pus layer inside the eye.

causes reduced smell, underdeveloped nose or eyes, and delayed puberty.

is a birth difference with urethral opening on the penis underside.

is a rare genetic condition causing hypospadias and developmental delay.

is a rare disorder causing absent thirst and dangerously high sodium levels.

is a rare brain growth causing laughing seizures and hormone changes.

is a tumor in the hypothalamus, affecting hormones, growth, and appetite.

is an underactive thyroid causing fatigue, weight gain, and cold sensitivity.