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Interpreting Your Search Results

Search results are displayed with informational links as follows:

= View a listing of laboratories that provide clinical testing for this disorder.
= View a listing of laboratories that provide testing on a research basis only.
= Read the GeneReview for this disorder.
= View and print relevant consumer health-oriented resources.

Search results appear in one or a combination of the following two formats:

1. Group(s) of Related Disorders

If your search term is a disorder that is included in a group of phenotypically related disorders or disorders caused by mutations in the same gene, the search result will display the group (see examples; note that the search term appears in bold). Each informational link is specific to the disorder it follows and to all disorders indented below it.

For example, the search term "tuberous sclerosis" will yield the following:

Tuberous Sclerosis Complex GeneReview tuberous sclerosis 30859 Resources 260699
   Tuberous Sclerosis 1 Clinical Tests 54046 Research Tests 54046
   Tuberous Sclerosis 2 Clinical Tests 54049 Research Tests 54049

Although phenotypically similar, tuberous sclerosis 1 and 2 are caused by mutations in different genes; tuberous sclerosis 1 and 2 are each followed by testing links specific to the genes causing them. The links to reviews and resources contain information about both TS1 and TS2.

Similarly, the search term "Tay-Sachs disease" will yield the following:

Hexosaminidase A Deficiency Clinical Tests 2283 Research Tests 2283 GeneReview tay-sachs 30827 Resources 228399
   Chronic and Adult-Onset Hexosaminidase A Deficiency
   Juvenile (Subacute) Hexosaminidase A Deficiency
   Tay-Sachs Disease

Tay-Sachs Disease, AB Variant [GM2 Activator Deficiency]   Clinical Tests 21210 Resources 2121099

Since the term "Tay-Sachs Disease" has no informational links following it, information on Tay-Sachs Disease is accessed via the links above it (following Hexosaminidase A Deficiency).

2. Alphabetical Listing

If the disease on which you are searching is not part of a group in the GeneTests database, the search result is an alphabetical list of disorders in which the search term figures, with informational links to testing, research, reviews, and resources where available. When a search yields results in a combination of formats, the disorders in a group display first; single entries follow in alphabetical order.

For example, the search term "Rickets" will yield the following:

Dent Disease   Clinical Tests 173676 Research Tests 173676 Resources 17367699
        Low-Molecular Weight Proteinuria with Nephrocalcinosis
        X-Linked Recessive Hypophosphatemic Rickets +/-Hypercalciuria
        X-Linked Recessive Nephrolithiasis
Hereditary Hypophosphatemic Rickets with Hypercalciuria   Clinical Tests 312582
Hypophosphatemic Rickets, Autosomal Recessive   Clinical Tests 310684
Hypophosphatemic Rickets, Dominant  Clinical Tests 29370 Resources 2937099
Hypophosphatemic Rickets, X-Linked Dominant   Clinical Tests 2755 Resources 275599
Pseudovitamin D Deficiency Rickets   Clinical Tests 55876 Resources 5587699
Rickets-Alopecia Syndrome   Clinical Tests 221547 Resources 22154799

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(Revised 3-3-09)



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