Clinical and research tests for A Du Moulinet D'hardemare - Genetic Testing Registry (GTR)

Results: 1 to 7 of 7

Select all conditions on this page	Conditions	Synonyms
Select item 41345	5p partial monosomy syndrome Tests Genes GeneReviews	5p deletion syndrome 5p minus syndrome 5p- syndrome Cat cry syndrome Chromosome 5p deletion syndrome Chromosome 5p- syndrome Cri du Chat Syndrome Monosomy 5p
Select item 53088	Wolman disease Tests Gene GeneReviews	Acid cholesteryl ester hydrolase deficiency, Wolman type Acid lipase disease CHOLESTEROL ESTER HYDROLASE DEFICIENCY, COMPLETE LAL DEFICIENCY, COMPLETE LIPA DEFICIENCY, COMPLETE LYSOSOMAL ACID LIPASE DEFICIENCY, ACUTE INFANTILE LYSOSOMAL ACID LIPASE DEFICIENCY, COMPLETE Wolman disease with hypolipoproteinemia and acanthocytosis Wolman disease, CESD
Select item 346432	Acromesomelic dysplasia 2B Tests Gene GeneReviews	Du pan syndrome Fibular hypoplasia and complex brachydactyly
Select item 40266	Cholesteryl ester storage disease Tests Gene GeneReviews
Select item 101814	T-lymphocyte deficiency Tests Genes GeneReviews	Immune defect due to absence of thymus Nezelof syndrome Thymic aplasia
Select item 1824050	Tooth agenesis, selective, 10 Tests Gene GeneReviews
Select item 41670	Duodenal ulcer Tests Genes GeneReviews	Duodenal ulcer (disease)

Results: 1 to 7 of 7

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