Genetic Testing for Severe Inherited Diseases, NGS

a.k.a.  ACY2 deficiency, aminoacylase 2 deficiency, Aspa deficiency, aspartoacylase deficiency, B variant GM2 gangliosidosis, beta hemoglobinopathies, beta type, Bloom syndrome, Bloom-Torre-Machacek syndrome, Bloom's syndrome, Canavan disease, Canavan's disease, cerebroside lipidosis syndrome, CF, classic galactosemia, congenital telangiectatic erythema, Cystic fibrosis, cystic fibrosis of pancreas, deficiency disease, epimerase deficiency galactosemia, erythroblastic anemia, FA, Fanconi anemia type C, Fanconi hypoplastic anemia, Fanconi pancytopenia, Fanconi panmyelopathy, fibrocystic disease of pancreas, Folling disease, Folling's disease, galactokinase deficiency disease, galactose epimerase deficiency, galactose-1-phosphate uridyl-transferase deficiency disease, galactosemia, GALE deficiency, GALK deficiency, GALT deficiency, ganglioside sialidase deficiency, Gaucher disease, Gaucher splenomegaly, Gaucher syndrome, Gaucher's disease, Gauchers disease, GD, glucocerebrosidase deficiency, glucocerebrosidosis, glucosyl cerebroside lipidosis, glucosylceramidase deficiency, glucosylceramide beta-glucosidase deficiency, glucosylceramide lipidosis, GM2 gangliosidosis, HexA deficiency, Hexosaminidase A deficiency, Hexosaminidase alpha-subunit deficiency (variant B), kerasin histiocytosis, kerasin lipoidosis, kerasin thesaurismosis, lipid histiocytosis, lipoid histiocytosis (kerasin type), Mediterranean anemia, microcytemia, ML4, MLIV, mucolipidosis type VI, mucoviscidosis, neuronal cholesterol lipidosis, neuronal lipidosis, Niemann-Pick disease types A and B, NPD, PAH deficiency, phenylalanine hydroxylase, Phenylalanine Hydroxylase Deficiency, phenylalanine hydroxylase deficiency, phenylalanine hydroxylase deficiency disease, phenylketonuria, PKU, sialolipidosis, Sphingolipidosis, sphingomyelin lipidosis, sphingomyelin/cholesterol lipidosis, sphingomyelinase deficiency, Tay-Sachs, Tay-Sachs disease], thalassemia, TSD, UDP-galactose-4-epimerase deficiency disease, UTP hexose-1-phosphate uridylyltransferase deficiency


Test information includes:

  • LOINC codes
  • diseases the test is often used to detect or monitor
  • overview of the test
  • utility - when/why/how the test is used
  • specimen collection methods/procedures
  • testing methodology
  • usual turnaround time
  • interpretation of test results
  • reference ranges for test results (normal, abnormal, etc.)
  • diagnosis and billing codes
    • ICD-10-CM
    • ICD-9-CM
    • CPT
  • additional or related tests
  • references - more information about the tests
  • web resources - additional online information about the test
  • search by test name, synonym, LOINC code, disease or CPT/ICD code
  • filter by Methodology or Specimen Type
  • auto-suggest search terms

This product also includes Laboratory Decision System (LDS) rankings. LDS uses a proprietary ranking system that enables healthcare providers to correctly select and order the most relevant tests based on diseases, symptoms, and ICD-10 codes.

Access to this feature is available in the following products:
  • Medical Lab Tests w/LDS Ranks

SAMPLE PAGE showing data for:  ABO Group and Rh Typing


Test Overview
Test Information
Billing/Diagnosis/LOINC Codes
Diseases/Conditions
Additional Tests
References
Web Resources
demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.