Clinical and research tests for 3,9-Dihydroeucomin - Genetic Testing Registry (GTR)

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Select all conditions on this page	Conditions	Synonyms
Select item 862913	Tumor predisposition syndrome 3	Glioma susceptibility 9 LONG TELOMERE SYNDROME, POT1-RELATED Melanoma, cutaneous malignant, susceptibility to, 10
Select item 7517	Medulloblastoma	MEDULLOBLASTOMA PREDISPOSITION SYNDROME Medulloblastoma, SUFU-Related Medulloblastoma, somatic
Select item 462538	Nephronophthisis 9
Select item 41678	Familial dysautonomia	FD HSAN 3 HSAN III HSN 3 Hereditary sensory and autonomic neuropathy 3 Hereditary sensory neuropathy type 3 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III Riley Day syndrome
Select item 355121	Cerebral cavernous malformation 3	Cerebral cavernous malformations 3 Familial Cerebral Cavernous Malformation 3
Select item 395635	Long QT syndrome 9
Select item 44131	Galactosylceramide beta-galactosidase deficiency	Galactocerebrosidase deficiency Globoid cell leukoencephalopathy Krabbe Disease Krabbe leukodystrophy Leukodystrophy, Globoid Cell
Select item 373335	Epilepsy, idiopathic generalized, susceptibility to, 3	EIG3 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, LOCUS ON CHROMOSOME 9 Epilepsy, idiopathic generalized 3
Select item 766800	Microcephaly 9, primary, autosomal recessive
Select item 382650	Osteoarthritis susceptibility 3	OSTEOARTHRITIS OF KNEE/HIP
Select item 90994	3-methylglutaconic aciduria type 1	3 alpha methylglutaconic aciduria type I 3 methylglutaconic aciduria type I 3 methylglutaconyl CoA hydratase deficiency 3MG CoA hydratase deficiency MGA type I
Select item 483324	Fanconi anemia complementation group C	FACC FANCONI PANCYTOPENIA, TYPE 3 Fanconi anemia, group C
Select item 1648400	Acyl-CoA dehydrogenase 9 deficiency	Acyl-CoA dehydrogenase family, member 9, deficiency of MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
Select item 320428	Mycobacterium tuberculosis, susceptibility to
Select item 87450	Oculocutaneous albinism type 3	ALBINISM III Albinism 3 Albinism, oculocutaneous, type III Rufous OCA Rufous albinism Rufous oculocutaneous albinism Xanthism
Select item 226942	Deficiency of hyaluronoglucosaminidase	HYALURONIDASE DEFICIENCY MPS IX Mucopolysaccharidosis Type IX Mucopolysaccharidosis type 9
Select item 482300	Pregnancy loss, recurrent, susceptibility to, 1	EMBRYONIC LOSS, RECURRENT FETAL LOSS, RECURRENT, SUSCEPTIBILITY TO MISCARRIAGE, RECURRENT STILLBIRTH, RECURRENT
Select item 9730	Acute myeloid leukemia	AML adult Acute granulocytic leukemia Acute myelogenous leukemia Acute myeloid leukemia, adult Acute non-lymphocytic leukemia Familial Acute Myelocytic Leukemia Leukemia, acute myelogenous, somatic Leukemia, acute myeloid, somatic
Select item 816204	Leukemia, acute lymphoblastic, susceptibility to, 3
Select item 483740	Non-acquired combined pituitary hormone deficiency with spine abnormalities	Combined pituitary hormone deficiency type 3 Deafness, sensorineural with pituitary dwarfism LHX3-Related Combined Pituitary Hormone Deficiency Pituitary hormone deficiency, combined with rigid cervical spine WBP syndrome Winkelman Bethge Pfeiffer syndrome Winkelmann-Bethge-Pfeiffer syndrome

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