is a long-lasting skin fungal infection causing warty growths after injury.

is a usually benign kidney tumor arising from renal tubules.

is a benign pituitary tumor, often nonfunctioning, causing vision and hormone issues.

is a kidney cancer subtype that often grows slowly and remains localized.

is a genetic condition where chromosomal changes cause early cataracts.

is a genetic chromosome disorder causing epilepsy and developmental differences.

involves missing pieces of chromosomes causing variable developmental and health challenges.

is a genetic condition from missing, extra, or altered chromosomes.

is a chromosomal condition causing overgrowth, birth differences, and medical complications.

is a genetic condition caused by extra chromosome material, affecting development.

is a rare genetic disorder causing developmental delays and multiple birth differences.

is a rare genetic disorder from 15q25 deletion, causing developmental delays.

is a genetic disorder causing developmental delay, learning challenges, and possible seizures.

is a rare genetic condition causing developmental delays and variable congenital features.

is a genetic condition from missing 17p13.1 DNA, causing variable developmental challenges.

is a rare genetic disorder causing developmental delay, learning difficulties, and anomalies.

is a rare genetic syndrome from extra 1p36.33 DNA, causing developmental delays.

is a rare condition from extra DNA on 22q13, causing developmental delays.

is a rare genetic disorder from a missing segment of chromosome 2.

is a rare genetic condition causing developmental delays and limb differences, variably.

is a rare chromosome 2 deletion causing limb differences and developmental delays.

is a rare inherited dementia causing progressive behavior and language changes.

is a rare chromosomal disorder causing developmental delays and variable features.

is a rare genetic disorder causing developmental delays and variable congenital differences.