Genetic Diseases

Color blindness is an impaired ability to adequately perceive certain colors that are heredit...

phenylketonuria( Felling's disease) - a serious hereditary disease caused by metabolic disord...

Teya-Sachs disease is a serious hereditary disease characterized by progressive motor disorde...

Fraser Syndrome - a combination of cryptophthalmos with urogenital and acrofacial anomalie...

Williams Syndrome is a fairly rare congenital genetic disease, manifested as a violation i...

Arnold Syndrome - Chiari( anomaly Arnold - Chiari) - congenital disorder of brain development...

Progeria is a rare genetic disease, first described by Guildford, which is manifested by prem...

Oxaluria( with the Greek oxalis - "sorrel", uron - "urine") is a disease caused by an increas...

Imperfect osteogenesis is a congenital disease of bones, as well as individual connective tis...