is a rare genetic disorder affecting brain connections and nerve function.

is a rare, usually harmless, congenital fatty growth in the corpus callosum.

is a rare brain tumor in the corpus callosum affecting adults.

is a common ovarian cyst after ovulation, often resolving spontaneously.

is loss of sight from brain’s visual cortex damage; eyes unaffected.

is a rare genetic condition causing cortical blindness, intellectual disability, polydactyly.

is a rare brain disorder causing hearing loss from auditory cortex damage.

is a rare TUBB3-related brain malformation causing developmental delays and coordination problems.

is an age-related lens clouding causing glare and blurry vision.

is a rare brain disorder causing progressive movement and thinking problems.

is an allergy to corticosteroids, leading to skin rashes or hives.

is a rare disorder affecting cortisol transport and stress hormone levels.

is a rare autoinflammatory disease causing sterile (aseptic) abscesses, steroid-responsive.

is a genetic disorder affecting cortisol activation, causing imbalance and androgen excess.

impairs cortisone-to-cortisol conversion, causing androgen excess, early puberty, and hirsutism.

is a rare genetic disorder reducing cortisol activation, causing androgen excess.

is a rare genetic condition from HRAS mutations, affecting growth and development.

is a type of asthma where chronic cough is the main symptom.

is a viral respiratory illness caused by SARS-CoV-2.

is an immune reaction to cow’s milk proteins, often in infants.

is a genetic disorder causing noncancerous growths (hamartomas) and higher cancer risk.

is a rare inherited disorder causing noncancerous growths and higher cancer risk.

is a rare inherited condition that raises the risk of certain tumors.

is a genetic condition causing multiple benign growths and increased cancer risks.