is a genetic condition causing thin enamel (hypoplasia), discoloration, and sensitivity.

is a genetic enamel-development disorder causing thin, fragile, discolored teeth.

is a genetic enamel-development disorder causing thin, weak, discolored teeth and sensitivity.

is a genetic enamel development disorder causing thin, fragile, discolored teeth.

is an inherited enamel development disorder causing weak, discolored, sensitive teeth.

is an inherited enamel formation disorder causing weak, discolored, easily damaged teeth.

is a genetic enamel disorder causing weak, discolored, and sensitive teeth.

is a genetic enamel disorder causing soft, discolored, easily worn teeth.

is an inherited enamel formation disorder causing fragile, sensitive, discolored teeth.

is a genetic enamel disorder causing fragile, discolored teeth from childhood.

is missing menstrual periods, from natural, hormonal, or medical causes.

is a lung infection from inhaling spores in bird or bat droppings.

is a parasitic infection spread by kissing bugs, affecting heart and gut.

is a group of inherited conditions affecting amino acid processing.

is a rare metabolic disorder causing seizures (epilepsy) and developmental problems.

is a rare genetic disorder causing developmental delay, seizures, and hypotonia.

is hearing loss from aminoglycoside antibiotics damaging inner-ear cells, often permanent.

is a birth defect pattern from early pregnancy methotrexate/aminopterin exposure.

is a rare genetic disorder causing microcephaly (small head) and early death.

is a rare inherited muscle disease causing severe weakness and breathing difficulties.

is a rare, life-threatening pregnancy emergency causing sudden breathing and heart failure.

is an immune reaction to amodiaquine causing rash, hives, or anaphylaxis.

is an intestinal infection causing diarrhea, stomach pain, and sometimes liver abscesses.

is a rare infection from environmental amoebae, affecting brain or eyes.