The Natural Repertory of Prof. William Nelson

Sandhoff disease (1) 5q13
Sanfilippo syndrome D (1) 12q14
*Sarcoma, synovial (2) Xp11.2
Scheie syndrome (1) 4p16.3
*SCID, X-Linked (2) Xq13.1-q21.1
Sclerotylosis (2) 4q28-q31
Seizures, benign neonatal (2) Chr.20
Severe combined immunodeficiency due to ADA deficiency (1) 20q13.11
Severe combined immunodeficiency due to IL-2 deficiency (1) 4q26-q27
Severe combined immunodeficiency (SCID), HLA class II-negative type (1) 19p13
?Sialidosis (1) Chr.10
?Sialidosis (2) 6p21.3
Sicle cell anemia (1) 11p15.5
?Situs inversus viscerum (2) 14q32
?SLE (1) 1q32
Small-cell cancer of lung (2) 3p23-p21
?Smith-Lemli-Opitz syndrome (2) 7q23-qter
Smith-Magenis syndrome (2) 17p11.2
Spastic paraplegia, X-Linked, uncomplicated (2) Xq21-q22
Spherocytosis, recessive (1) 1q21
Spherocytosis-1 (3) 14q22-q23.2
Spherocytosis-2 (3) 8p11.2
Spinal muscular atrophy II (2) 5q11.2-q13.3
Spinal muscular atrophy III (2) 5q11.2-q13.3
Spinocerebellar-ataxia 6p21.3-p21.2
Spondyloepiphyseal dysplasia congenital (3) 12q13.11-q13.2
*Spondyloepiphyseal dysplasia tarda (2) Xp22
Stickler syndrome (3) 12q13.11-q13.2
Sucrose intolerance (1) 3q25-q26
?Susceptibility to amyloid in FMF (1) 11pter-p12
Tay-Sachs disease (1) 15q22-q25.1
Testicular feminization (1) Xcen-q13
Thalassemias, alpha- (1) 16pter-p13.3
Thalassemias, beta- (1) 11p15.5
Thrombocytopenia, X-Linked (2) Xp21-p11
Thrombophilia due to elevated HRG (2) 3p14-qter
Thrombophilia due to excessive plasminogen activator inhibitor (1) 7q21.3-q22
Thrombophilia due to heparin cofactor II deficiency (1) Chr.22
Thyroid hormone resistance (3) 3p24.3
Thyroid iodine peroxidase deficiency (1) 2pter-p12
Thyroid papillary carcinoma (1) 10q11-q12
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