The Natural Repertory of Prof. William Nelson

Cataract, zonular pulverulent (2) 1q22
*?Cataracts, congenital total (2) Xp
Central core disease of muscle (2) 19q12-q13.2
Cerebral amyloid angiopathy (1) Chr.20
Cerebrotendinous xanthomatosis (2) 2q33-qter
[CEPT-deficiency] (1) 16q21
Charcot-Marie-Tooth disease, slow nerve conduction type Ia (2) 17p11.2
Charcot-Marie-Tooth disease, slow nerve conduction type Ib (2) 1q21.2-q23
Charcot-Marie-Tooth disease, X-linked dominant (2) Xq13
Charcot-Marie Tooth disease X-linked recessive 1 (2) Xq22.2
?Chediak-Higashi syndrome (2) 1q43
Cholesteryl ester storage disease (1) 10q24-q25
*Chondrodysplasia punctata, X-Linked dominant (2) Xq28
Chondrodysplasia punctata, X-Linked recessive (2) Xpter-p22.32
Choroideremia (2) Xq21.2
Chronic granulomatous disease due to deficiency of NCF-1 (1) 7q11.23
Chronic granulomatous disease due to deficiency of NCF-2 (1) 1q25
Chronic infections (1) 10q11.2-q21
Citrullinemia (1) 9q34
Cleft palate, X-linked (2) Xq21
CMO II deficiency (1) 8q21
*Coffin-Lowry syndrome (2) Xp22.2-p22.1
?Coloboma of iris (2) 2pter-p25.1
Colorblindness, blue monochromatic (3) Xq28
Colorblindness, blue monochromatic (3) Xq28
Colorblindness, blue monochromatic (3 Xq28
Colorblindness, deutan (3) Xq28
Colorblindness, protan (3) Xq28
Colorblindness, tritan (2) 7q22-qter
Colorectal adenoma (1) 12p12.1
?Colorectal cancer (1) 12p12.1
Colorectal cancer (1) 18q23.3
Colorectal cancer (3) 17p13.1
Colorectal cancer, familial (2) 5q22-q23
Combined C6/C7 deficiency (1) 5p13
?Combined variable hypogammaglobulinemia (1) 14q32.33
Conductive deafness with stapes fixation (2) Xq13-q21.1
Coproporphyria (1) Chr.9
{Coronary artery disease, susceptibility to} (1) 6q27
Cortisol resistance (1) 5q31
CR1 deficiency (1) 1q32
217