Ooocx

Huntington disease

Phenylketonuria Parkinson's disease, familial

Muscular dystrophy, limb-girdle, type 2E

Severe combined immunodeficiency

Coagulation factor XI

Achondroplasia

Dopamine receptor

Cri-du-chat syndrome, mental retardation Taste receptor

Anemia, megaloblastic

Mast cell leukemia Germ cell tumors

Polycystic kidney disease, adult, type II

Hair color, red

Colorectal cancer

Coagulation factor XII (Hageman factor)

Leigh syndrome Hirschsprung disease Severe combined immunodeficiency Dwarfism

Diphtheria toxin receptor

Coagulation factor XIII

Maple syrup urine disease, type Ib

Tumor necrosis factor (cachectin) Retinitis pigmentosa

Startle disease, autosomal dominant and recessive

Gluten-sensitive enteropathy (celiac disease)

Diabetes mellitus, insulin-dependent

Hemochromatosis

Macular dystrophy

203 million bases

Pancreatitis, hereditary

194 million bases

Estrogen receptor

Parkinson disease, juvenile, type 2

183 million bases

Deafness, autosomal recessive Moebius syndrome

Lambert-Eaton syndrome

Severe combined immunodeficiency disease, Athabascan

Spastic paraplegia

Sickle cell anemia Cyclin-dependent H Thalassemias, beta kinase inhibitor

Osteoporosis Deafness, autosomal recessive

Taste receptors

Colorectal cancer Adrenoleukodystrophy

Rickets, vitamin D-resistant

Split hand/foot malformation, type 3

Diabetes mellitus, insulin-dependent

Glaucoma

Multiple myeloma

Phenylketonuria

McArdle disease

Alcohol intolerance, acute

144 million bases

144 million bases

143 million bases

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