Mendelian Modes of Inheritance

1. X Linked Recessive

1.1. R retts syndrome

1.2. A alpot syndrome

1.3. V vitamin D resistant rickets

1.4. I incontinentia pigmenti

2. X Linked Dominant

2.1. Lady lesh nyhan syndrome

2.2. Hardinge hemophilia A and B, hunters

2.3. disease

2.4. college colour blindness

2.5. Girls G6PD deficiency

2.6. Dont duchenne muscular dystrophy

2.7. Care chronic granulomatous disease

2.8. About agammaglobulinemia

2.9. Foolish fabrys disease, fragile X

2.10. syndrome

2.11. Words wiscott aldrich syndrome

3. Autosomal Dominance

3.1. He Has A Very DOMINANT Father

3.2. H Huntington's Disease

3.3. H hereditary spherocytosis

3.4. A adult onset polycystic kidney disease

3.5. V VWD

3.6. D Dystrophic myotonic

3.7. O osteogenesis imperfecta

3.8. M marfans syndrome

3.9. I intermittent porphyria

3.10. N Neurofibromatosis 1 (NF1):

3.11. A Achondroplasia

3.12. N Neurofibromatosis 2 (NF2)

3.13. T tuberous sclerosis

3.14. F familial hypercholestrolemia

3.15. familial adenamatous polyposis

4. Autosomal Recessive

4.1. A alpha 1 antitrypsin, ataxia

4.2. telangiectasia, alkaptonuria

4.3. B beta thalassemia, sick cell anemia

4.4. C cystic fibrosis, congenital adrenal

4.5. hypoplasia

4.6. D deafness

4.7. E emphysema

4.8. F Fredric's ataxia

4.9. G gauchers disease, glycogen storage

4.10. disease

4.11. G galactosemia

4.12. H hemochromatosis, homocystinuria

4.13. I inborn error of metabolism