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Fanconi anemia complementation group D1

MeSH: C563980ORPHA: 319462

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

Fanconi anemia that has material basis in homozygous or compound heterozygous mutation in the BRCA2 gene on chromosome 13q13

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

C563980

Orphanet Code

ORPHA:319462
Fanconi anemia complementation group D1
MeSHC563980
OrphanetORPHA:319462
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
Fanconi anemia complementation group D1 | OrphanDrug