Clinical and research tests for 3,7-Dimethylocta-1,6-dien-3-ol - Genetic Testing Registry (GTR)

Results: 1 to 17 of 17

Select all conditions on this page	Conditions	Synonyms
Select item 382217	NPHP3-related Meckel-like syndrome	Dandy-Walker cyst with renal-hepatic-pancreatic dysplasia GOLDSTON SYNDROME Meckel syndrome type 7 NPHP3-Related Meckel Syndrome
Select item 48574	Schizophrenia
Select item 41523	Type 2 diabetes mellitus	DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST Diabetes mellitus, noninsulin-dependent, late onset KCNJ11-Related Susceptibility to Noninsulin-Dependent Diabetes Mellitus Type II diabetes mellitus
Select item 237026	Papillary renal cell carcinoma type 1	Papillary Renal Carcinoma RENAL CELL CARCINOMA, PAPILLARY, 1, SOMATIC Renal adenocarcinoma Renal cell carcinoma 1 Renal cell carcinoma, somatic
Select item 389187	Hepatocellular carcinoma	Hepatocellular cancer Hepatoma LIVER CELL CARCINOMA Primary carcinoma of liver
Select item 765974	Emery-Dreifuss muscular dystrophy 7, autosomal dominant	Emery-Dreifuss muscular dystrophy 7, AD
Select item 347272	Gamma-glutamylcysteine synthetase deficiency	ANEMIA, CONGENITAL, NONSPHEROCYTIC HEMOLYTIC, 7 Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to
Select item 462293	Long QT syndrome 2
Select item 78631	Congenital secretory diarrhea, chloride type	CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE Chloridorrhea, congenital Congenital chloride diarrhea Darrow-Gamble disease Diarrhea 1, secretory chloride, congenital Familial Chloride Diarrhea
Select item 357420	Polysyndactyly 4	Polysyndactyly uncomplicated Preaxial Polydactyly Type IV Preaxial polydactyly 4
Select item 406292	Frontonasal dysplasia	Frontonasal dysplasia sequence Median facial cleft syndrome
Select item 863898	Progeroid features-hepatocellular carcinoma predisposition syndrome	Ruijs-Aalfs syndrome
Select item 124355	Nocturnal enuresis	BEDWETTING Enuresis nocturna
Select item 83428	Colorectal cancer	Colorectal cancer, somatic Malignant Colorectal Neoplasm
Select item 370149	Malaria, susceptibility to
Select item 1633554	Lynch syndrome
Select item 75781	Hereditary antithrombin deficiency	Antithrombin III deficiency Antithrombin deficiency Reduced antithrombin III activity Thrombophilia due to antithrombin III deficiency

Results: 1 to 17 of 17

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