Hereditary diseases, also known as inherited diseases or genetic disorders, are diseases which can be passed down through generations of the same family. The following is a list of hereditary disorders
Achondroplasia
Acid Maltase Deficiency
Albinism
Angelman Syndrome
Canavan Disease
Charcot-Marie-Tooth Disease
Color Blindness
Cri du Chat Syndrome
Down Syndrome
Duchenne Muscular Dystrophy
Fragile X Syndrome
Galactosemia
Gilbert's Syndrome
Hemophilia
Hereditary Fructose Intolerance
Hereditary Hemochromatosis
Hereditary Spherocytosis
Joubert Syndrome
Klinefelter Syndrome
Krabbe Disease
Lesch-Nyhan Syndrome
Marfan Syndrome
Muscular Dystrophy
Myotonic Dystrophy
Nail-Patella Syndrome
Neurofibromatosis
Noonan Syndrome
Pelizaeus-Merzbacher Disease
Phenylketonuria
Polycystic Kidney Disease
Porphyria
Prader-Willi Syndrome
Prune Belly Syndrome
Retinoblastoma
Rett Syndrome
Rubinstein-Taybi Syndrome
Russell Silver Syndrome
Sanfilippo Syndrome
Shwachman Syndrome
Smith-Magenis Syndrome
Spina bifida
Stickler Syndrome
TAR Syndrome
Tay-Sachs Disease
Tay-Sachs Syndrome
Turner Syndrome
Usher Syndrome
Usher Syndrome
Variegate Porphyria
Von Hippel-Lindau Syndrome
Waardenburg Syndrome
Wilson's Disease
Wolf-Hirschhorn Syndrome
Xeroderma Pigmentosum
XXX Syndrome
XXXX Syndrome - Rare genetic disorder in females caused by the presence of four X chromosomes rather than two.
XYY Syndrome - XYY syndrome is characterized by an extra copy of the Y chromosome in each of a male's cells.
YY Syndrome - A genetic condition where males have an extra Y chromosome (i.e XYY) in each of their cells.
Achondroplasia
Acid Maltase Deficiency
Albinism
Angelman Syndrome
Canavan Disease
Charcot-Marie-Tooth Disease
Color Blindness
Cri du Chat Syndrome
Down Syndrome
Duchenne Muscular Dystrophy
Fragile X Syndrome
Galactosemia
Gilbert's Syndrome
Hemophilia
Hereditary Fructose Intolerance
Hereditary Hemochromatosis
Hereditary Spherocytosis
Joubert Syndrome
Klinefelter Syndrome
Krabbe Disease
Lesch-Nyhan Syndrome
Marfan Syndrome
Muscular Dystrophy
Myotonic Dystrophy
Nail-Patella Syndrome
Neurofibromatosis
Noonan Syndrome
Pelizaeus-Merzbacher Disease
Phenylketonuria
Polycystic Kidney Disease
Porphyria
Prader-Willi Syndrome
Prune Belly Syndrome
Retinoblastoma
Rett Syndrome
Rubinstein-Taybi Syndrome
Russell Silver Syndrome
Sanfilippo Syndrome
Shwachman Syndrome
Smith-Magenis Syndrome
Spina bifida
Stickler Syndrome
TAR Syndrome
Tay-Sachs Disease
Tay-Sachs Syndrome
Turner Syndrome
Usher Syndrome
Usher Syndrome
Variegate Porphyria
Von Hippel-Lindau Syndrome
Waardenburg Syndrome
Wilson's Disease
Wolf-Hirschhorn Syndrome
Xeroderma Pigmentosum
XXX Syndrome
XXXX Syndrome - Rare genetic disorder in females caused by the presence of four X chromosomes rather than two.
XYY Syndrome - XYY syndrome is characterized by an extra copy of the Y chromosome in each of a male's cells.
YY Syndrome - A genetic condition where males have an extra Y chromosome (i.e XYY) in each of their cells.
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