The Natural Repertory of Prof. William Nelson

Hydrocephalus, X-Linked (2) Xq28
Hydrops fetalis, 1 form (1) 19cen-q12
Hyperammonemia due to CTPase deficiency (1) 1pter-q12
Hyperbetalipoproteinemia (1) 2p24
Hypercholesterolemia, familial (3) 19p13.2-p13.1
?Hyperglycinemia, isolated nonketotic, type I (2) 9p22
?Hypergonadotropic hypogonadism (1) 19q13.32
?Hyperimmunoglobulin G1syndrome (2) 14q32.33
Hyperkalemic periodic paralysi (3) 17q23.1-q25.3
?Hyperleucinemia-isoleucinemia or hypervalinemia (1) 12pter-q12
Hyperlipoproteinemia I (1) 8p22
Hyperlipoproteinemia, type Ib (1) 19q13.1
Hyperlipoproteinemia, type III (1) 19q13.1
[Hyperphenylalaninemia, mild] (3) 12p24.1
[?Hyperproglucagonemia] (1) 2q36-q37
Hyperproinsulinemia, familial (1) 11p15.3
Hypertriglyceridemia, 1 form (1) 11q23
Hypertrophic cardiomyopathy, 1 form (3) 14q12
?Hypervalinemia or hyperleucine-isoleucinemia (1) Chr.19
Hypobetalipoproteinemia 11q23
Hypobetalipoproteinemia (1) 2p24
[Hypoceruloplasminemia, hereditary] (1) 3q21-q24
Hypofibrinogenemia, gamma types (1) 4q28
?Hypogonadotropic hypogonadism due to GNRH deficiency (1) 8p21-q11.2
Hypomagnesemia, X-Linked primary (2) Xp22
?Hypomelanosis of Ito (2) 15q11-q13
?Hypomelanosis of Ito (2) 9q33-qter
Hypoparathyroidism, familial (1) 11p15.3-p15.1
*Hypoparathyroidism, X-Linked (2) Xq26-q27
?Hypophosphatasia, adult (1) 1p36.1-p34
Hypophosphatasia, infantile (3) 1p36.1-p34
Hypophosphatemia, hereditary (2) Xp22.2-p22.1
?Hypophosphatemia with deafness (2) Xp22
Hypoprothrombinemia (1) 11p11-q12
Hypothyroidism, hereditary congenital, 1 or more types (1) 8q24.224.3
Hypothyroidism, nongoitrous (1) 1p22
Hypothyroidism, nongoitrous, due to TSH resistance (1) 14q31
?Ichthyosis vulgaris (1) 1q21
Ichthyosis, X-Linked (3) Xpter-p22.32
Immunodeficiency, X-Linked, with hyperIgM (2) Xq24-q27
*Incontinentia pigmenti, familial (2) Xq27-q28
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