is an autism spectrum condition affecting social communication, interests, and behavior.

is a fungal infection or allergy from Aspergillus, mainly involving the lungs.

is newborn oxygen deprivation around birth, causing breathing problems and organ injury.

is a rare genetic skeletal disorder causing narrow chest and breathing problems.

is a rare inherited skeletal disorder causing narrow chest and breathing problems.

is a rare genetic disorder causing narrow chest and breathing difficulties.

is a rare genetic ciliopathy causing narrow chest, breathing problems, skeletal abnormalities.

is a rare inherited skeletal disorder causing small chest and breathing problems.

is lung inflammation from inhaled stomach contents, causing cough and breathing difficulty.

is an immune reaction to aspirin causing hives, breathing trouble, or anaphylaxis.

is chronic asthma, nasal polyps, and reactions to aspirin-like pain relievers.

is a disorder with intact vision but impaired object recognition and naming.

is the loss of recognizing objects by touch (tactile agnosia).

is a chronic airway inflammation causing wheezing, breathlessness, cough, and flare-ups.

is a respiratory condition combining asthma, nasal polyps, and aspirin/NSAID sensitivity.

is an eye condition causing blurred vision from irregular corneal curvature.

is a rare genetic skeletal disorder causing short stature and bone abnormalities.

is a tick-borne rickettsial infection causing fever, headache, and rash.

is a rare glial brain tumor in children and young adults.

is a rare brain tumor with MN1 gene changes, often in youth.

is a brain tumor that starts in star-shaped support cells.

is a slow-growing, low-grade brain tumor with an IDH mutation.

is a malignant brain tumor with IDH gene mutation.

is an aggressive IDH-mutant glioma, a grade 4 brain tumor.