is a rare genetic disorder causing retinal, brain, bone, and gastrointestinal problems.

is an occupational asthma triggered by cobalt exposure, causing wheezing.

is a skin allergy causing itchy, red rash from cobalt exposure.

is a rare genetic brain malformation causing developmental delays, seizures, vision problems.

is a brain disorder causing cobblestone cortex (lissencephaly), sparing muscles and eyes.

is a common, benign peripheral retinal change, usually asymptomatic and incidental.

is a substance use disorder causing compulsive cocaine use, cravings, and harm.

results from prenatal cocaine exposure causing growth restriction and developmental problems.

is acute cocaine toxicity causing agitation, chest pain, high blood pressure.

is a fungal lung infection causing flu-like illness; sometimes spreads bodywide.

is an intestinal parasitic infection causing diarrhea, cramps, and dehydration.

is inner ear (cochlear) disorder causing hearing loss and tinnitus.

is underdevelopment or absence of the hearing nerve, causing severe hearing loss.

is a rare inherited disorder causing hearing loss (sensorineural) and cataracts.

is a congenital inner ear structural abnormality affecting hearing and balance.

is a rare genetic disorder causing growth failure, photosensitivity, and neurologic decline.

is a rare disorder causing poor growth, developmental delays, and premature aging.

is a rare inherited disorder with severe growth, neurological, and photosensitivity features.

is a milder, later-onset genetic disorder causing photosensitivity and neurodevelopmental issues.

is a rare genetic condition causing developmental delays and multi-system anomalies.

is a rare parasitic infection causing cysts, often in brain and nerves.

is a rare condition that limits cell energy and causes varied symptoms.

is a genetic mitochondrial disorder causing energy deficiency, affecting muscles, brain, kidneys.

is a rare genetic condition causing developmental delay and physical differences.