How many genetic disorers can you list? List them.?

Answer 1

Achromatopsia
Adrenal Hypoplasia Congenita
Adrenoleukodystrophy
Aicardi Syndrome
Albinism/Hypopigmentation
Alexander Disease
Alpers' Disease
Alpha-1 Antitrypsin Deficiency
Alzheimer's Disease
Amblyopia
Angelman Syndrome
Anencephaly
Aniridia
Anophthalmia
Ataxia Telangiectasia
Autism
Bardet-Biedl Syndrome
Barth Syndrome
Batten Disease
Best's Disease
Bipolar Disorder
Bloom Syndrome
Branchio-Oto-Renal (BOR) Syndrome
Canavan Syndrome
Cancer Genetics
Carnitine Deficiencies
Carnitine Acylcarnitine Translocase Deficiency
Carnitine Palmitoyltransferase Deficiency
Cerebral Palsy


Charcot-Marie-Tooth Disease


Cleft Lip/Cleft Palate


Coffin Lowry Syndrome


Coloboma


Color Blindness


Congenital Heart Defects


Congenital Hip Dysplasia (Dislocation)


Connective Tissue Disorders


Cooley's Anemia


Corneal Dystrophy


Cornelia de Lange Syndrome


Cystic Fibrosis


Cystinosis


Diabetes


Down Syndrome


Duane Syndrome


Ehlers-Danlos Syndrome


Epidermolysis Bullosa


Familial Dysautonomia


Familial Mediterranean Fever


Fibrodysplasia Ossificans Progressiva


Fragile X Syndrome


G6PD (Glucose-6-Phosphate Dehydrogenase) Deficiency Anemia


Galactosemia


Gaucher Disease


Gilbert's Syndrome


Glaucoma


Hemochromatosis


Hemoglobin C Disease


Hemophilia/Bleeding Disorders


Hirschsprung's Disease


Homocystinuria


Huntington's Disease


Hurler Syndrome


Juvenile Retinoschisis (X Linked)


Klinefelter Syndrome


Leber Congenital Amaurosis


Lipid Storage Diseases


Long Q-T Syndrome


Macular Degeneration


Marfan Syndrome


Marshall Syndrome


McCune-Albright Syndrome


Menkes Disease


Metabolic Disorders


Microphthalmus


Mitochondrial Disease


Mucolipidoses


Mucopolysaccharide Disorders


Muscular Dystrophy


Neonatal Onset Multisystem Inflammatory Disease


Neural Tube Defects


Neurofibromatosis


Niemann-Pick Disease


Noonan Syndrome


Optic Atrophy


Osteogenesis Imperfecta


Peutz-Jeghers Syndrome


Phenylketonuria (PKU)


Polycystic Kidney Disease


Pseudoxanthoma Elasticum


Progeria


Ptosis


Rentinitis Pigmentosa


Scheie Syndrome


Schizophrenia


Sickle Cell Anemia


Smith-Magenis Syndrome


Skeletal Dysplasias


Spherocytosis


Spina Bifida


Spinocerebellar Ataxia


Stargardt Disease (Macular Degeneration)


Stickler Syndrome


Tay-Sachs Disease


Thalassemia


Treacher Collins Syndrome


Tuberous Sclerosis


Turner's Syndrome


Urea Cycle Disorder


Usher's Syndrome


Velocardiofacial Syndrome


von Hippel-Lindau Disease


Werner Syndrome


Williams Syndrome


Xeroderma Pigmentosum


XXX Syndrome


XYY Syndrome