is a rare, severe skeletal disorder, usually life-limiting around birth.

is a rare genetic skeletal disorder, often life-limiting before or after birth.

is a rare genetic disorder causing brainstem malformation and cranial nerve dysfunction.

is kidney damage from tiny cholesterol crystals blocking small renal arteries.

is a rare genetic disorder affecting blood vessels, hearing, diabetes, seizures, kidneys.

is a congenital absence of the thyroid gland, causing severe hypothyroidism.

is an overgrowth disorder with distinctive facial features and developmental delays.

is an immune reaction to Atlantic cod proteins, causing skin, breathing, anaphylaxis.

is an allergy to Atlantic salmon, causing hives, swelling, or anaphylaxis.

is a chronic, itchy skin disease causing dryness, rash, and flares.

is a chronic, itchy eczema causing dry skin and recurrent flares.

is a long-term eczema causing dry, itchy, inflamed skin flares.

is a chronic, itchy, inflamed skin condition with genetic predisposition.

is a chronic, itchy skin inflammation influenced by genes and environment.

is a chronic, itchy skin condition with dry, inflamed, eczema-like patches.

is a chronic, itchy eczema causing dry, inflamed skin flares.

is a genetic form of eczema causing chronic itchy, inflamed skin.

is a genetic eczema subtype causing chronic itch, dryness, and inflammation.

is a chronic allergic eye inflammation linked to atopic dermatitis.

is a rare inherited lysosomal disorder causing progressive childhood neurodegeneration, seizures.

is a rare, inherited neurodegenerative disorder causing early, progressive parkinsonism.

is a rare congenital blockage of the urethra causing urinary obstruction.

is a heart defect of atrial appendages, raising arrhythmia and stroke risk.

is an irregular heart rhythm causing palpitations, fatigue, and stroke risk.