Get paginated list of products | Enigma Genomics

{
  "code": 200,
  "data": [
    {
      "tat": "20-25 business days",
      "price_b2c": "2550",
      "package_name": "Comprehensive Premarital Screening (7500 Conditions)",
      "product_code": "EGEXOPRE",
      "analysis_name": "Short Variants (SNVs & Indels) and Copy Number Variation (CNV)",
      "price_b2c_usd": "680",
      "disease_tested": "",
      "brief_description": "Comprehensive Premarital Screening provides prospective couples with a comprehensive assessment of their genetic carrier status with detailed recommendations on how to ensure the well-being of their future children.",
      "brief_description_ar": ""
    },
    {
      "tat": "7-10 business days",
      "price_b2c": "950",
      "package_name": "Noninvasive prenatal testing (NIPT)",
      "product_code": "EGCRRNIP",
      "analysis_name": "Short Variants and CNV Analysis",
      "price_b2c_usd": "285",
      "disease_tested": "Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), Trisomy 13 (Patau syndrome), Turner syndrome (Monosomy X), Klinefelter syndrome (XXY), and other sex chromosome aneuploidies.",
      "brief_description": "The Non-Invasive Prenatal Testing is a genetic screening that can be performed during pregnancy to assess the risk of certain chromosomal abnormalities in a developing fetus using a maternal blood sample.",
      "brief_description_ar": ""
    },
    {
      "tat": "20-30 business days",
      "price_b2c": "2550",
      "package_name": "Comprehensive Cancer Panel",
      "product_code": "EGCANALL",
      "analysis_name": "Short Variants and CNV Analysis",
      "price_b2c_usd": "765",
      "disease_tested": "ataxia-telangiectasia (A-T)\r\nBloom syndrome\r\nCarney complex\r\nconstitutional mismatch repair deficiency (CMMR-D)\r\nCostello syndrome\r\nCowden and Cowden-like syndrome\r\nDICER1 syndrome\r\ndyskeratosis congenita\r\nfamilial acute myeloid leukemia (AML) syndrome\r\nfamilial adenomatous polyposis (FAP)\r\nfamilial gastrointestinal stromal tumors (GIST)\r\nfamilial isolated pituitary adenoma (FIPA)\r\nfamilial neuroblastoma\r\nfamilial platelet disorder with propensity to myeloid malignancy (FPD/AML)\r\nFanconi anemia\r\nGATA2 deficiency\r\nGorlin syndrome (nevoid basal cell carcinoma)\r\nhereditary breast and ovarian cancer syndrome (HBOC)\r\nhereditary diffuse gastric cancer (HGDC)\r\nhereditary papillary renal cell carcinoma\r\nhereditary paraganglioma-pheochromocytoma syndrome (PGL/PCC)\r\njuvenile polyposis syndrome (JPS)\r\nLi-Fraumeni syndrome (LFS)\r\nLynch syndrome – also known as hereditary non-polyposis colorectal cancer (HNPCC)\r\nmelanoma-pancreatic cancer syndrome (M-PCS)\r\nmultiple endocrine neoplasia type 1 (MEN1)\r\nmultiple endocrine neoplasia type 2 (MEN2)\r\nMUTYH-associated polyposis (MAP)\r\nneurofibromatosis type 1 (NF1)\r\nneurofibromatosis type 2 (NF2)\r\nNijmegen breakage syndrome (NBS)\r\noligodontia-colorectal cancer syndrome\r\nPerlman syndrome\r\nPeutz-Jeghers syndrome (PJS)\r\nretinoblastoma\r\nrhabdoid tumor predisposition syndrome (RTPS)\r\nSimpson-Golabi-Behmel syndrome (SGBS)\r\ntuberous sclerosis complex (TSC)\r\nvon Hippel-Lindau syndrome (VHL)\r\nWerner syndrome\r\nWilms tumor-related conditions",
      "brief_description": "This panel analyzes 157 Genes and is designed to maximize diagnostic yield for individuals with a personal or family history of mixed cancers affecting multiple organ systems.",
      "brief_description_ar": ""
    }
  ],
  "page": 1,
  "count": 3,
  "message": "Products list fetched successfully",
  "records": 5
}

The List Products API retrieves detailed information about products on the Enigma platform associated with the authenticated user.

Authentication

x-api-keystring

API Key authentication via header

Path parameters

pagestringRequired

(Required)

recordsstringRequired

(Required)

Query parameters

searchKeystringOptional

searchValuestringOptional

sortInstringOptional

Response

codeinteger

datalist of objects

pageinteger

countinteger

messagestring

recordsinteger

$	curl -G https://api.enigmagenomics.com/products/1/5 \
>	-H "x-api-key: <apiKey>" \
>	-d searchKey=string \
>	-d searchValue=string \
>	-d sortIn=desc