ProductGuru Free barcode & product database

Mendelian inheritance in man: catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Johns Hopkins Press Mendelian inheritance in man: catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes is a computer science identified by EAN 9780801815935.

9780801815935 Certainty 75%
  • Brand: Johns Hopkins Press
  • Category: computer science
  • Barcode type: EAN-13 / GTIN-13
  • GS1 registered country: Bookland (ISBN-13)
  • Data confidence: 75%

Product Details

Barcode (EAN/GTIN)9780801815935
Product nameMendelian inheritance in man: catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes
Brand / ManufacturerJohns Hopkins Press
Categorycomputer science
GS1 Prefix978 — registered in Bookland (ISBN-13)
Barcode typeEAN-13 / GTIN-13
Data certainty75%

Verified Product Facts

The barcode 9780801815935 passes the GS1 mod-10 check-digit test, so it is a structurally valid GTIN. Its 978 prefix was issued by the GS1 member organisation for Bookland (ISBN-13) — registration, not place of manufacture.

Recorded specifications

Item weight666 grams
ManufacturerJohns Hopkins University Press
Number of items1
Package dimensions200 × 15 × 250 millimeters (L×W×H)
Package weight666 grams
Product dimensions200 × 15 × 250 millimeters (L×W×H)
UNSPSC code55101500

Attributes as recorded in the product catalogue data we hold. Figures describe the packaged article and may differ between production batches.

Buy this product

As an Amazon Associate and eBay Partner we earn from qualifying purchases. Prices and availability are set by the retailer and verified on their site.

⊞ Compare this product
🟢 No recall found for this barcode  ·  We matched this barcode against recall records from EU Safety Gate, Health Canada, US FDA, Transport Canada and 18 other national safety agencies (2026-10-01). Not every recall notice lists a barcode, so this is not a safety guarantee — check the brand owner or the regulator for the definitive record. Browse recalls by agency, country or year →

More from Johns Hopkins Press

Barcode Lookup API

Access this product programmatically via the ProductGuru free API:

GET https://myproduct.guru/scan/9780801815935
GET https://myproduct.guru/api/search?q=9780801815935

No API key required. Returns JSON with product name, brand, manufacturer, and more.

About EAN Barcode 9780801815935

Barcode 9780801815935 is a EAN-13 (GTIN-13) identifying Mendelian inheritance in man: catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes in the GS1 global system.

  • Barcode format: EAN-13 / GTIN-13 — 13-digit globally unique product identifier
  • GS1 prefix 978: assigned to companies registered in Bookland (ISBN-13)
  • Manufacturer: Johns Hopkins Press
  • Scan compatibility: readable by any smartphone barcode scanner app

Frequently Asked Questions

What product has barcode 9780801815935?

Barcode 9780801815935 is Mendelian inheritance in man: catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes, sold under the brand Johns Hopkins Press.

Who manufactures barcode 9780801815935?

Johns Hopkins Press is recorded as the manufacturer of Mendelian inheritance in man: catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes (barcode 9780801815935).

What country is barcode 9780801815935 from?

Based on the GS1 prefix 978, this product was registered in Bookland (ISBN-13).

Is barcode 9780801815935 a valid EAN?

Yes, 9780801815935 is a valid EAN-13 barcode with correct check digit.

⚠️ Data Disclaimer

Data is aggregated from open datasets and may be inaccurate or out of date; some outbound links are affiliate links from which we may earn a commission.

Imprint  |  Terms of Service  |  Privacy Policy  |  Imprint

Found wrong info? Report it

Reports are queued for human review. We don't store this data for marketing.

Was this page helpful?