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The Natural Repertory of Prof. William Nelson

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ALPHABETICAL INDEX OF HEALTH DISORDERS<br />

AND CHROMOSOME LOCATION<br />

Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency (1) 8q21<br />

Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency (3) 6p21.3<br />

3-hydroxyacyl-CoA dehydrogenase deficiency (1) Chr.7<br />

*46, XY female (2) xp22.2-p21.3<br />

Aarskog-Scott syndrome (2) Xq13<br />

?Abetaa Lipoproteinemia 2p24<br />

[Acanthocytosis 1 form] (1) 17q21-q22<br />

Acatalasemia (1) 11p13<br />

Acetyl-CoA carboxylase deficiency (1) 17q21<br />

Acid-maltase deficiency, adult (1) 17q23<br />

Acoustic neuroma (2) 22q11.21-q13.1<br />

?Acrokeratoelastoidosis (2) 2p<br />

ACTH deficiency (1) 2p25<br />

Acute alcohol intolerance (1) 12q24.2<br />

Acute Lymphoblastic Leukemia (2) 9p22-p21<br />

Acute Promyelocytic Leukemia (1) 17q21.1<br />

Acute Promyelocytic Leukemia (2) 15q22<br />

Acyl-CoA Dehydrogenase, medium chain, deficiency <strong>of</strong> (1) 1p31<br />

Acyl-CoA Dehydrogenase, short chain, deficiency <strong>of</strong> (1) 12q22-qter<br />

Adenylosuccinase deficiency (1) Chr.22<br />

Adrenal hyperplasia II (1) 1p13<br />

Adrenal hypoplasia, primary (2) Chr.10<br />

Adrenocortical carcinoma (2) Xp21.3-p21.2<br />

Adrenoleukodystrophy (2) 11p15.5<br />

Adrenomyeloneruopathy (2) Xq28<br />

[AFP deficiency, congenital] (1) Xq28<br />

Agammaglobulinemia, type 2, X-linked (2) 4q11-q13<br />

*Agammaglobulinemia, X-Linked (2) Xq21.3-q22<br />

Aicardi syndrome (2) Xq22<br />

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