U.S. flag

An official website of the United States government

Results: 1 to 20 of 35

Make selection to find tests for any of the checked conditions.[x]
ConditionsSynonyms
Hereditary spherocytosis type 4
  • Hemolytic Anemia due to Band 3 Montefiore
  • SLC4A1-Related Hereditary Spherocytosis
  • SLC4A1-Related Spherocytosis
  • Spherocytosis type 4
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
Deficiency of steroid 11-beta-monooxygenase
  • 11-alpha beta-hydroxylase deficiency
  • 11-beta-Hydroxylase-Deficient Congenital Adrenal Hyperplasia
  • 11-beta-hydroxylase deficiency
  • ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE DEFICIENCY
  • Adrenal hyperplasia 4
  • Adrenal hyperplasia IV
  • Adrenal hyperplasia hypertensive form
  • Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
  • P450c11b1 deficiency
  • Steroid 11-beta-hydroxylase deficiency
Hereditary angioedema type 3
  • ANGIONEUROTIC EDEMA, HEREDITARY, WITH NORMAL C1 INHIBITOR CONCENTRATION AND FUNCTION
  • ESTROGEN-RELATED HAE
  • ESTROGEN-SENSITIVE HAE
  • HAE WITH NORMAL C1 INHIBITOR CONCENTRATION AND FUNCTION
  • Hereditary angioedema, type III
Hyperuricemic nephropathy, familial juvenile type 4
  • TUBULOINTERSTITIAL KIDNEY DISEASE, AUTOSOMAL DOMINANT, 5
Keratosis follicularis
  • Darier disease
  • Darier's disease
  • Darier-White Disease
Pontocerebellar hypoplasia type 2B
  • TSEN2-Related Pontocerebellar Hypoplasia
Adams-Oliver syndrome 4
BLOOD GROUP, MN
Spermatogenic failure 4
  • AZOOSPERMIA WITH MATURATION ARREST
  • Arrest of spermatogenesis
  • Azoospermia due to Perturbations of Meiosis
  • PREGNANCY LOSS 4
  • Spermatogenesis arrest
Adams-Oliver syndrome 3
Syndactyly type 3
  • Ring and little finger syndactyly
  • SYNDACTYLY OF FINGERS IV AND V
  • Syndactyly of fingers four and five
  • Syndactyly of the ring and little finger
  • Syndactyly, Type III
Spondyloepimetaphyseal dysplasia, PAPSS2 type
  • BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES
  • SEMD, PAKISTANI TYPE
  • Spondyloepimetaphyseal dysplasia, pakistani type
Preeclampsia/eclampsia 4
Maraviroc response
  • Selzentry response
Cerebral cavernous malformation 4
  • Cerebral cavernous malformations 4
  • Familial Cerebral Cavernous Malformation 4
Thyroid cancer, nonmedullary, 3
Sofosbuvir response
  • Sovaldi response
Susceptibility to angioedema induced by ACE inhibitors
Bifunctional peroxisomal enzyme deficiency
  • D-bifunctional enzyme deficiency
  • D-bifunctional protein deficiency
  • DBP deficiency
  • Pseudo Zellweger syndrome

Results: 1 to 20 of 35

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.