is a rare inherited disorder affecting fat breakdown and many body systems.

is a rare genetic disorder that affects brain, liver, and development.

is a group of inherited disorders affecting cellular fat breakdown.

is a genetic disorder affecting peroxisomes, often causing seizures and developmental problems.

is a rare inherited disorder of peroxisomes causing multi-system developmental problems.

is a rare inherited disorder affecting peroxisomes, causing serious developmental problems.

is a rare inherited disorder disrupting peroxisome formation, impacting multiple organs.

is a rare inherited Zellweger spectrum disorder affecting multiple organs and development.

is a rare inherited disorder affecting brain, liver, and body development.

is a rare genetic disorder affecting brain, liver, and development.

is a rare inherited peroxisomal disorder causing multi-organ dysfunction from infancy.

is a rare inherited disorder affecting brain, liver, and other organs.

is a genetic disorder affecting peroxisomes, causing developmental delays and organ dysfunction.

is a rare genetic disorder affecting multiple organs, causing severe developmental problems.

is a rare inherited condition affecting peroxisome formation, causing body-wide problems.

is a rare inherited disorder affecting brain, liver, and other organs.

is a rare inherited condition affecting peroxisome formation and multiple organs.

is a rare genetic disorder affecting peroxisomes, causing severe early multi-organ problems.

is a rare genetic disorder affecting peroxisome function, causing multi-system problems.

is a rare genetic disorder affecting brain, liver, hearing, and vision.

is a rare genetic disorder causing defective peroxisomes and multi-system disease.

causes childhood hearing loss and, in females, ovarian insufficiency; sometimes neurological problems.

is a rare inherited condition causing hearing loss and ovarian problems.

is a rare inherited disorder causing hearing loss and ovarian problems.