is a rare genetic condition affecting learning, communication, behavior, and facial development.

is a rare genetic syndrome causing learning difficulties and several physical changes.

is a rare genetic condition affecting learning, hand growth, and the jaw.

is a genetic condition causing developmental delay, heart problems, and loose joints.

is a condition causing intellectual disability, cataracts, ear calcification, and myopathy.

is a rare genetic condition affecting learning, growth, and brain development.

is a genetic syndrome with intellectual disability, facial differences, and undescended testes.

is a rare disorder causing developmental delay, intellectual disability, and contractures.

is a genetic syndrome causing intellectual disability, distinct features, hypogonadism, and diabetes.

is a rare genetic disorder causing developmental delay, cataracts, and microcephaly.

is a rare condition causing intellectual disability, seizures, and movement problems.

is a rare genetic condition affecting learning, speech, and facial features.

is a genetic condition causing developmental delay, learning problems, and facial differences.

is a genetic condition causing intellectual disability, facial differences, and hand anomalies.

is a rare genetic condition causing intellectual disability, abnormal movements, and ataxia.

is a rare genetic condition causing intellectual disability and brain differences.

is a genetic condition causing developmental delay, low muscle tone, and anomalies.

is a genetic condition causing developmental delay, macrocephaly, and hypotonia.

is a rare genetic condition causing learning problems, muscle weakness, short stature.

causes developmental delays, muscle weakness, short height, and hormone problems.

is a rare genetic disorder causing intellectual disability, obesity, and brain/facial differences.

is a rare condition affecting learning, weight, facial features, eyes, and skin.

is a rare genetic condition with intellectual disability, polydactyly, and uncombable hair.

causes intellectual disability, seizures, walking problems, and distinctive facial features.